Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 83988 |
|---|---|
| ensemblid | ENSG00000104490.18 |
| hgncid | 7655 |
| symbol | NCALD |
| name | neurocalcin delta |
| refseq_nuc | NM_032041.3 |
| refseq_prot | NP_114430.2 |
| ensembl_nuc | ENST00000220931.11 |
| ensembl_prot | ENSP00000220931.6 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 101686542 |
| end | 101790969 |
| strand | - |
| ver | v1.2 |
| region | chr8:101686542-101790969 |
| region5000 | chr8:101681542-101795969 |
| regionname0 | NCALD_chr8_101686542_101790969 |
| regionname5000 | NCALD_chr8_101681542_101795969 |
| 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 | 193 | 300 | 82 | 50 | 130 | 2 | 34 | 96 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| 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 | 582 | 299 | 82 | 50 | 129 | 2 | 34 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| c0002 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| 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 | 2895 | 116 | 28 | 28 | 47 | 1 | 12 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0002 | 0/1 | 2895 | 52 | 4 | 11 | 31 | 0 | 5 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0003 | 0/0 | 2895 | 27 | 0 | 4 | 16 | 0 | 7 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0004 | 0/0 | 2895 | 20 | 7 | 2 | 5 | 1 | 5 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0005 | 0/0 | 2890 | 14 | 9 | 0 | 4 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0006 | 1/0 | 2895 | 13 | 0 | 0 | 12 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0007 | 0/0 | 2895 | 10 | 8 | 0 | 0 | 0 | 2 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0008 | 0/0 | 2896 | 9 | 0 | 0 | 9 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0009 | 0/0 | 2895 | 7 | 7 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0010 | 0/0 | 2895 | 6 | 3 | 2 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0011 | 0/0 | 2895 | 3 | 3 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0012 | 0/0 | 2895 | 3 | 0 | 2 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0013 | 0/0 | 2895 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0014 | 0/0 | 2895 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0015 | 0/0 | 2895 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0016 | 0/0 | 2895 | 2 | 1 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0017 | 0/0 | 2895 | 2 | 0 | 0 | 2 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0018 | 0/0 | 2891 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0019 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0020 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0021 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0022 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0023 | 0/0 | 2896 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0024 | 0/0 | 2896 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0025 | 0/0 | 2896 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| t0026 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| 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 | 3 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| 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 | 582 | 299 | 82 | 50 | 129 | 2 | 34 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0002 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3476 | 116 | 28 | 28 | 47 | 1 | 12 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0002 | 0/1 | 3476 | 52 | 4 | 11 | 31 | 0 | 5 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0003 | 0/0 | 3476 | 27 | 0 | 4 | 16 | 0 | 7 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0004 | 0/0 | 3476 | 20 | 7 | 2 | 5 | 1 | 5 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0005 | 0/0 | 3471 | 14 | 9 | 0 | 4 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0006 | 1/0 | 3476 | 13 | 0 | 0 | 12 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0007 | 0/0 | 3476 | 10 | 8 | 0 | 0 | 0 | 2 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0008 | 0/0 | 3477 | 9 | 0 | 0 | 9 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0009 | 0/0 | 3476 | 7 | 7 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0010 | 0/0 | 3476 | 6 | 3 | 2 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0011 | 0/0 | 3476 | 3 | 3 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0012 | 0/0 | 3476 | 2 | 0 | 2 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0013 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0014 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0015 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0016 | 0/0 | 3476 | 2 | 1 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0017 | 0/0 | 3476 | 2 | 0 | 0 | 2 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0018 | 0/0 | 3472 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0019 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0020 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0021 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0022 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0023 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0024 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0025 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0001t0026 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| a0001c0002t0012 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | copy fasta | chr8 | 101681542 | 101795969 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0008g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0009g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0010g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0010g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0010g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0010g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0010g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0012g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0012g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0013g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0013g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0014g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0014g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0015g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0015g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0016g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0016g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0017g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0017g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0018g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0018g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0019g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0020g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0021g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0022g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0023g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0024g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0025g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0001t0026g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| a0001c0002t0012g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00423 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0151 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0292 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0081 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01069 | hp2 | a0001 | c0001 | t0016 | g0197 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01074 | hp1 | a0001 | c0001 | t0010 | g0247 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01081 | hp2 | a0001 | c0001 | t0012 | g0029 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01106 | hp2 | a0001 | c0001 | t0012 | g0053 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | IBS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0078 | EUR | IBS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0279 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02080 | hp1 | a0001 | c0001 | t0024 | g0068 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0243 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0110 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0262 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0271 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0275 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0189 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0153 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0108 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02622 | hp1 | a0001 | c0001 | t0018 | g0245 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02647 | hp1 | a0001 | c0001 | t0026 | g0158 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0269 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0281 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02809 | hp1 | a0001 | c0001 | t0015 | g0027 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0291 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0287 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0286 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0260 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0155 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0263 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0259 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0272 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03098 | hp2 | a0001 | c0001 | t0025 | g0159 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0258 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0282 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0266 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0250 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03516 | hp1 | a0001 | c0001 | t0016 | g0089 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0109 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03669 | hp1 | a0001 | c0001 | t0023 | g0052 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03710 | hp1 | a0001 | c0001 | t0010 | g0217 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0168 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0169 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0086 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0060 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18522 | hp2 | a0001 | c0001 | t0018 | g0065 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | CHB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0070 | EAS | CHB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18947 | hp2 | a0001 | c0001 | t0017 | g0044 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18953 | hp1 | a0001 | c0001 | t0019 | g0046 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18966 | hp1 | a0001 | c0001 | t0008 | g0139 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18969 | hp1 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0132 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18981 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18984 | hp2 | a0001 | c0002 | t0012 | g0146 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18991 | hp1 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19009 | hp1 | a0001 | c0001 | t0008 | g0091 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | LWK | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19062 | hp2 | a0001 | c0001 | t0017 | g0051 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19065 | hp2 | a0001 | c0001 | t0021 | g0122 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19068 | hp1 | a0001 | c0001 | t0008 | g0190 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19080 | hp2 | a0001 | c0001 | t0008 | g0242 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0251 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ASW | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0111 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0288 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0285 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0294 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | USA | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| HG06807 | hp2 | a0001 | c0001 | t0014 | g0252 | AFR | USA | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | USA | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | USA | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0101 | AFR | LWK | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | LWK | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0066 | REF | REF | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0208 | REF | REF | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
| 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 |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:101719258
|
G | A | 1 | a0001c0002 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.372C>T | p.Ile124Ile | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/4 | 499/3476 | 372/582 | 124/193 | chr8 | 101719258 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:101686827
|
C | T | 2 | a0001c0001t0012a0001c0002t0012 | 3 | HG01081.hp2 HG01106.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2482G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 2482 | chr8 | 101686827 | |||||
| chr8:101687033
|
T | C | 1 | a0001c0001t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2276A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 2276 | chr8 | 101687033 | |||||
| chr8:101687490
|
T | C | 1 | a0001c0001t0021 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1819A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1819 | chr8 | 101687490 | |||||
| chr8:101687501
|
G | T | 2 | a0001c0001t0016a0001c0001t0025 | 3 | HG01069.hp2 HG03098.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1808C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1808 | chr8 | 101687501 | |||||
| chr8:101687777
|
C | T | 1 | a0001c0001t0014 | 2 | HG06807.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1532G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1532 | chr8 | 101687777 | |||||
| chr8:101687938
|
G | T | 1 | a0001c0001t0024 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1371C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1371 | chr8 | 101687938 | |||||
| chr8:101688002
|
C | T | 1 | a0001c0001t0004 | 20 | HG00738.hp1 HG01167.hp2 HG01515.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1307G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1307 | chr8 | 101688002 | |||||
| chr8:101688067
|
T | C | 6 | a0001c0001t0002a0001c0001t0010a0001c0001t0012others(3): Show | 63 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1242A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1242 | chr8 | 101688067 | |||||
| chr8:101688100
|
T | C | 6 | a0001c0001t0002a0001c0001t0010a0001c0001t0012others(3): Show | 63 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1209A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1209 | chr8 | 101688100 | |||||
| chr8:101688103
|
G | A | 2 | a0001c0001t0003a0001c0001t0017 | 29 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1206C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1206 | chr8 | 101688103 | |||||
| chr8:101688268
|
T | G | 1 | a0001c0001t0015 | 2 | HG02615.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1041A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1041 | chr8 | 101688268 | |||||
| chr8:101688310
|
A | G | 2 | a0001c0001t0007a0001c0001t0020 | 11 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*999T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 999 | chr8 | 101688310 | |||||
| chr8:101688408
|
A | T | 5 | a0001c0001t0002a0001c0001t0012a0001c0001t0019others(2): Show | 57 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*901T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 901 | chr8 | 101688408 | |||||
| chr8:101688581
|
TTTTTA | T | 3 | a0001c0001t0005a0001c0001t0018a0001c0001t0022 | 17 | HG02027.hp1 HG02280.hp1 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*723_*727delTAAAA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 723 | chr8 | 101688581 | |||||
| chr8:101688815
|
C | G | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 494 | chr8 | 101688815 | |||||
| chr8:101688889
|
C | T | 2 | a0001c0001t0016a0001c0001t0025 | 3 | HG01069.hp2 HG03098.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*420G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 420 | chr8 | 101688889 | |||||
| chr8:101688895
|
G | A | 2 | a0001c0001t0016a0001c0001t0025 | 3 | HG01069.hp2 HG03098.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 414 | chr8 | 101688895 | |||||
| chr8:101688908
|
T | C | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | 287 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*401A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 401 | chr8 | 101688908 | |||||
| chr8:101688909
|
T | C | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | 287 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*400A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 400 | chr8 | 101688909 | |||||
| chr8:101688926
|
T | A | 1 | a0001c0001t0017 | 2 | NA18947.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*383A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 383 | chr8 | 101688926 | |||||
| chr8:101689101
|
C | T | 1 | a0001c0001t0011 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*208G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 208 | chr8 | 101689101 | |||||
| chr8:101689138
|
G | A | 1 | a0001c0001t0022 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 171 | chr8 | 101689138 | |||||
| chr8:101689203
|
C | T | 1 | a0001c0001t0013 | 2 | HG02976.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*106G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 106 | chr8 | 101689203 | |||||
| chr8:101689228
|
C | CA | 5 | a0001c0001t0008a0001c0001t0018a0001c0001t0023others(2): Show | 14 | HG00423.hp2 HG02080.hp1 HG02523.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*80dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 80 | chr8 | 101689228 | |||||
| chr8:101689246
|
G | A | 1 | a0001c0001t0009 | 7 | HG02258.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*63C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 63 | chr8 | 101689246 | |||||
| chr8:101689293
|
T | C | 1 | a0001c0001t0026 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 16 | chr8 | 101689293 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:101689460
|
C | T | 1 | a0001c0001t0004g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.485-54G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689460 | ||||||
| chr8:101689641
|
C | T | 42 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(39): Show | 42 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.485-235G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689641 | ||||||
| chr8:101689683
|
A | C | 1 | a0001c0001t0004g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.485-277T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689683 | ||||||
| chr8:101689730
|
G | T | 32 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(29): Show | 32 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.485-324C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689730 | ||||||
| chr8:101689744
|
T | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0009others(56): Show | 60 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.485-338A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689744 | ||||||
| chr8:101689822
|
G | A | 97 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(94): Show | 98 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.485-416C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689822 | ||||||
| chr8:101689933
|
G | A | 73 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(70): Show | 75 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.485-527C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689933 | ||||||
| chr8:101689950
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.485-544A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689950 | ||||||
| chr8:101689959
|
C | T | 82 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(79): Show | 84 | HG00423.hp2 HG00639.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.485-553G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689959 | ||||||
| chr8:101690179
|
C | CCTTT | 93 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(90): Show | 93 | HG00423.hp2 HG00639.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.485-774_485-773ins others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690179 | ||||||
| chr8:101690379
|
A | C | 190 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(187): Show | 194 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.485-973T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690379 | ||||||
| chr8:101690433
|
C | T | 1 | a0001c0001t0020g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.485-1027G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690433 | ||||||
| chr8:101690470
|
C | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.485-1064G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690470 | ||||||
| chr8:101690509
|
A | G | 261 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(258): Show | 265 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(262): Show |
intron_variant | MODIFIER | c.485-1103T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690509 | ||||||
| chr8:101690599
|
A | G | 3 | a0001c0001t0007g0278a0001c0001t0007g0279a0001c0001t0007g0285 | 3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.485-1193T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690599 | ||||||
| chr8:101690829
|
G | C | 1 | a0001c0001t0002g0295 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.485-1423C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690829 | ||||||
| chr8:101690934
|
C | T | 1 | a0001c0001t0020g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.485-1528G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690934 | ||||||
| chr8:101690935
|
G | A | 5 | a0001c0001t0001g0059a0001c0001t0001g0079a0001c0001t0001g0147others(2): Show | 5 | HG01952.hp2 HG02132.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-1529C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690935 | ||||||
| chr8:101691106
|
C | A | 1 | a0001c0001t0020g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484+1685G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691106 | ||||||
| chr8:101691223
|
C | T | 124 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 127 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.484+1568G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691223 | ||||||
| chr8:101691250
|
A | AC | 7 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0196others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+1540dupG | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691250 | ||||||
| chr8:101691254
|
C | G | 2 | a0001c0001t0007g0168a0001c0001t0007g0250 | 2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.484+1537G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691254 | ||||||
| chr8:101691452
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0079 | 2 | HG01952.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.484+1339C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691452 | ||||||
| chr8:101691588
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.484+1203A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691588 | ||||||
| chr8:101691722
|
A | G | 163 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 164 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.484+1069T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691722 | ||||||
| chr8:101691758
|
T | C | 1 | a0001c0001t0005g0018 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.484+1033A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691758 | ||||||
| chr8:101692014
|
C | T | 1 | a0001c0001t0003g0222 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.484+777G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692014 | ||||||
| chr8:101692278
|
C | T | 94 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 96 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.484+513G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692278 | ||||||
| chr8:101692302
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.484+489G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692302 | ||||||
| chr8:101692328
|
C | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 69 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.484+463G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692328 | ||||||
| chr8:101692342
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(80): Show | 83 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.484+449T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692342 | ||||||
| chr8:101692468
|
C | A | 2 | a0001c0001t0001g0267a0001c0001t0007g0291 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.484+323G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692468 | ||||||
| chr8:101692610
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.484+181G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692610 | ||||||
| chr8:101692644
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.484+147G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692644 | ||||||
| chr8:101692737
|
C | T | 33 | a0001c0001t0002g0002a0001c0001t0002g0163a0001c0001t0003g0024others(30): Show | 34 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.484+54G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692737 | ||||||
| chr8:101692957
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0228others(4): Show | 7 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-61A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101692957 | ||||||
| chr8:101693000
|
C | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-104G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693000 | ||||||
| chr8:101693219
|
C | T | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.379-323G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693219 | ||||||
| chr8:101693246
|
G | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0219 | 3 | HG04184.hp1 NA18948.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.379-350C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693246 | ||||||
| chr8:101693315
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-419C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693315 | ||||||
| chr8:101693318
|
G | GT | 14 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0174others(11): Show | 14 | HG00438.hp1 HG01081.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.379-423dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
G | GTT | 24 | a0001c0001t0001g0013a0001c0001t0002g0009a0001c0001t0002g0014others(21): Show | 24 | HG00597.hp2 HG00621.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.379-424_379-423dup others(2): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
G | GTTT | 17 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0049others(14): Show | 17 | HG00423.hp1 HG01952.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.379-425_379-423dup others(3): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GT | G | 31 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0032others(28): Show | 31 | HG00735.hp2 HG00738.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.379-423delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GTT | G | 33 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0047others(30): Show | 33 | HG01109.hp1 HG01257.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-424_379-423del others(2): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GTTT | G | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.379-425_379-423del others(3): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GTTTT | G | 8 | a0001c0001t0001g0130a0001c0001t0001g0221a0001c0001t0007g0284others(5): Show | 8 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-426_379-423del others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.379-438_379-423del others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GTTTTTTT others(10): Show |
G | 35 | a0001c0001t0002g0002a0001c0001t0002g0163a0001c0001t0002g0170others(32): Show | 36 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.379-439_379-423del others(17): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0003g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.379-440_379-423del others(18): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GTTTTTTT others(12): Show |
G | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.379-441_379-423del others(19): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693318
|
GTTTTTTT others(14): Show |
G | 38 | a0001c0001t0001g0095a0001c0001t0001g0138a0001c0001t0001g0140others(35): Show | 38 | HG00639.hp1 HG01069.hp2 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.379-443_379-423del others(21): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | ||||||
| chr8:101693322
|
T | G | 1 | a0001c0001t0009g0001 | 3 | HG03139.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.379-426A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693322 | ||||||
| chr8:101693323
|
T | G | 3 | a0001c0001t0009g0155a0001c0001t0009g0260a0001c0001t0009g0262 | 3 | HG02258.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.379-427A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693323 | ||||||
| chr8:101693351
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.379-455A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693351 | ||||||
| chr8:101693369
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0007g0291 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.379-473G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693369 | ||||||
| chr8:101693406
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0007g0291 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.379-510G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693406 | ||||||
| chr8:101693418
|
C | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(11): Show | 14 | HG01109.hp2 HG02074.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.379-522G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693418 | ||||||
| chr8:101694008
|
C | T | 181 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(178): Show | 185 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(182): Show |
intron_variant | MODIFIER | c.379-1112G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694008 | ||||||
| chr8:101694012
|
A | AC | 188 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(185): Show | 192 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.379-1117_379-1116i others(3): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694012 | ||||||
| chr8:101694089
|
G | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-1193C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694089 | ||||||
| chr8:101694219
|
G | A | 101 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 103 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.379-1323C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694219 | ||||||
| chr8:101694289
|
G | A | 1 | a0001c0001t0003g0191 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.379-1393C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694289 | ||||||
| chr8:101694336
|
C | A | 258 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(255): Show | 262 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(259): Show |
intron_variant | MODIFIER | c.379-1440G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694336 | ||||||
| chr8:101694390
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(168): Show | 173 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.379-1494A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694390 | ||||||
| chr8:101694429
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.379-1533T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694429 | ||||||
| chr8:101694462
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.379-1566G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694462 | ||||||
| chr8:101694593
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0007g0291 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.379-1697C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694593 | ||||||
| chr8:101694754
|
C | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(245): Show | 252 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(249): Show |
intron_variant | MODIFIER | c.379-1858G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694754 | ||||||
| chr8:101694838
|
C | T | 1 | a0001c0001t0009g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.379-1942G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694838 | ||||||
| chr8:101695036
|
C | T | 6 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0009g0001others(3): Show | 8 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2140G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695036 | ||||||
| chr8:101695358
|
T | C | 1 | a0001c0001t0003g0135 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.379-2462A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695358 | ||||||
| chr8:101695419
|
T | C | 11 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0005g0021others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.379-2523A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695419 | ||||||
| chr8:101695846
|
A | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0087a0001c0001t0001g0120others(1): Show | 4 | HG04184.hp1 NA18948.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-2950T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695846 | ||||||
| chr8:101695967
|
T | G | 1 | a0001c0001t0016g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.379-3071A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695967 | ||||||
| chr8:101696080
|
C | G | 6 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0009g0001others(3): Show | 8 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-3184G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696080 | ||||||
| chr8:101696143
|
T | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(159): Show | 164 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.379-3247A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696143 | ||||||
| chr8:101696525
|
C | T | 1 | a0001c0001t0010g0281 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.379-3629G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696525 | ||||||
| chr8:101696526
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.379-3630C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696526 | ||||||
| chr8:101696533
|
G | A | 1 | a0001c0001t0005g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.379-3637C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696533 | ||||||
| chr8:101696708
|
T | C | 1 | a0001c0001t0020g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379-3812A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696708 | ||||||
| chr8:101696819
|
T | C | 1 | a0001c0001t0025g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.379-3923A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696819 | ||||||
| chr8:101696825
|
T | TA | 78 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 78 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.379-3930dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696825 | ||||||
| chr8:101696927
|
G | A | 7 | a0001c0001t0004g0261a0001c0001t0010g0081a0001c0001t0010g0217others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-4031C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696927 | ||||||
| chr8:101697183
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.379-4287C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697183 | ||||||
| chr8:101697316
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-4420G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697316 | ||||||
| chr8:101697374
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.379-4478C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697374 | ||||||
| chr8:101697706
|
T | G | 7 | a0001c0001t0004g0261a0001c0001t0010g0081a0001c0001t0010g0217others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-4810A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697706 | ||||||
| chr8:101697919
|
T | C | 78 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 78 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.379-5023A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697919 | ||||||
| chr8:101698048
|
C | A | 1 | a0001c0001t0001g0293 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.379-5152G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698048 | ||||||
| chr8:101698259
|
G | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-5363C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698259 | ||||||
| chr8:101698318
|
C | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-5422G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698318 | ||||||
| chr8:101698433
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.379-5537A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698433 | ||||||
| chr8:101698481
|
G | C | 7 | a0001c0001t0004g0261a0001c0001t0010g0081a0001c0001t0010g0217others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-5585C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698481 | ||||||
| chr8:101699079
|
G | GA | 255 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(252): Show | 259 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(256): Show |
intron_variant | MODIFIER | c.379-6184dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699079 | ||||||
| chr8:101699079
|
G | GAA | 16 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0185others(13): Show | 16 | HG00423.hp2 HG01109.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.379-6185_379-6184d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699079 | ||||||
| chr8:101699100
|
G | A | 4 | a0001c0001t0016g0089a0001c0001t0016g0197a0001c0001t0025g0159others(1): Show | 4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-6204C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699100 | ||||||
| chr8:101699203
|
T | A | 274 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(271): Show | 278 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(275): Show |
intron_variant | MODIFIER | c.379-6307A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699203 | ||||||
| chr8:101699242
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-6346T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699242 | ||||||
| chr8:101699353
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.379-6457G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699353 | ||||||
| chr8:101699416
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(162): Show | 167 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.379-6520A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699416 | ||||||
| chr8:101699461
|
T | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0039others(7): Show | 11 | HG01257.hp2 HG01258.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.379-6565A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699461 | ||||||
| chr8:101699699
|
G | A | 169 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(166): Show | 171 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(168): Show |
intron_variant | MODIFIER | c.379-6803C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699699 | ||||||
| chr8:101699762
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-6866C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699762 | ||||||
| chr8:101699789
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.379-6893A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699789 | ||||||
| chr8:101699969
|
G | A | 168 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(165): Show | 170 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.379-7073C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699969 | ||||||
| chr8:101699990
|
G | T | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.379-7094C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699990 | ||||||
| chr8:101700028
|
T | TTTTA | 97 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0039others(94): Show | 99 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.379-7136_379-7133d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700028 | ||||||
| chr8:101700028
|
TTTTA | T | 8 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0157others(5): Show | 8 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-7136_379-7133d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700028 | ||||||
| chr8:101700056
|
A | ATTTATTT others(1): Show |
8 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0132others(5): Show | 8 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-7161_379-7160i others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700056 | ||||||
| chr8:101700056
|
A | T | 7 | a0001c0001t0001g0185a0001c0001t0001g0267a0001c0001t0007g0291others(4): Show | 9 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-7160T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700056 | ||||||
| chr8:101700118
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(169): Show | 174 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(171): Show |
intron_variant | MODIFIER | c.379-7222A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700118 | ||||||
| chr8:101700412
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.379-7516C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700412 | ||||||
| chr8:101700439
|
A | G | 1 | a0001c0001t0004g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.379-7543T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700439 | ||||||
| chr8:101700529
|
G | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0031others(67): Show | 71 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.379-7633C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700529 | ||||||
| chr8:101700576
|
C | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(159): Show | 164 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.379-7680G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700576 | ||||||
| chr8:101700587
|
G | A | 5 | a0001c0001t0008g0091a0001c0001t0008g0132a0001c0001t0008g0137others(2): Show | 5 | NA18966.hp1 NA18970.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-7691C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700587 | ||||||
| chr8:101700646
|
A | G | 163 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(160): Show | 165 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.379-7750T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700646 | ||||||
| chr8:101700666
|
T | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(253): Show | 260 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(257): Show |
intron_variant | MODIFIER | c.379-7770A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700666 | ||||||
| chr8:101700929
|
G | T | 4 | a0001c0001t0016g0089a0001c0001t0016g0197a0001c0001t0025g0159others(1): Show | 4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-8033C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700929 | ||||||
| chr8:101701012
|
G | A | 29 | a0001c0001t0001g0093a0001c0001t0002g0182a0001c0001t0004g0060others(26): Show | 29 | HG01069.hp2 HG01167.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.379-8116C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701012 | ||||||
| chr8:101701068
|
T | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(253): Show | 260 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(257): Show |
intron_variant | MODIFIER | c.379-8172A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701068 | ||||||
| chr8:101701163
|
C | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0005g0021others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.379-8267G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701163 | ||||||
| chr8:101701177
|
G | A | 8 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0132others(5): Show | 8 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-8281C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701177 | ||||||
| chr8:101701178
|
A | G | 2 | a0001c0001t0002g0040a0001c0001t0002g0134 | 2 | NA18956.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.379-8282T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701178 | ||||||
| chr8:101701184
|
G | A | 1 | a0001c0001t0005g0249 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.379-8288C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701184 | ||||||
| chr8:101701186
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.379-8290A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701186 | ||||||
| chr8:101701242
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.379-8346G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701242 | ||||||
| chr8:101701270
|
C | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0005g0021others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-8374G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701270 | ||||||
| chr8:101701308
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0007g0291 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.379-8412A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701308 | ||||||
| chr8:101701320
|
G | A | 7 | a0001c0001t0004g0261a0001c0001t0010g0081a0001c0001t0010g0217others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-8424C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701320 | ||||||
| chr8:101701458
|
A | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.379-8562T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701458 | ||||||
| chr8:101701656
|
T | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0219 | 3 | HG04184.hp1 NA18948.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.379-8760A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701656 | ||||||
| chr8:101701657
|
T | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0219 | 3 | HG04184.hp1 NA18948.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.379-8761A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701657 | ||||||
| chr8:101701699
|
G | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(253): Show | 260 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(257): Show |
intron_variant | MODIFIER | c.379-8803C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701699 | ||||||
| chr8:101702077
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-9181C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702077 | ||||||
| chr8:101702108
|
A | C | 14 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(11): Show | 16 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.379-9212T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702108 | ||||||
| chr8:101702141
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.379-9245T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702141 | ||||||
| chr8:101702195
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.379-9299G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702195 | ||||||
| chr8:101702201
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.379-9305A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702201 | ||||||
| chr8:101702291
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0083 | 2 | HG01257.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.379-9395G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702291 | ||||||
| chr8:101702327
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.379-9431C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702327 | ||||||
| chr8:101702718
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-9822C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702718 | ||||||
| chr8:101702735
|
G | A | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.379-9839C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702735 | ||||||
| chr8:101702742
|
T | C | 264 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(261): Show | 268 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(265): Show |
intron_variant | MODIFIER | c.379-9846A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702742 | ||||||
| chr8:101702775
|
C | G | 14 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(11): Show | 16 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.379-9879G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702775 | ||||||
| chr8:101702792
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0219 | 3 | HG04184.hp1 NA18948.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.379-9896A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702792 | ||||||
| chr8:101702793
|
T | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-9897A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702793 | ||||||
| chr8:101702797
|
G | A | 1 | a0001c0001t0004g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.379-9901C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702797 | ||||||
| chr8:101702820
|
T | G | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.379-9924A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702820 | ||||||
| chr8:101702822
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-9926A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702822 | ||||||
| chr8:101702898
|
C | A | 1 | a0001c0001t0002g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.379-10002G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702898 | ||||||
| chr8:101703120
|
C | T | 1 | a0001c0001t0002g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.379-10224G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703120 | ||||||
| chr8:101703152
|
C | CT | 21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(18): Show | 23 | HG00639.hp2 HG01243.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.379-10257dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703152 | ||||||
| chr8:101703152
|
CT | C | 67 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(64): Show | 67 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.379-10257delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703152 | ||||||
| chr8:101703165
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.379-10269A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703165 | ||||||
| chr8:101703389
|
A | ACAGGACA others(8): Show |
4 | a0001c0001t0007g0285a0001c0001t0010g0281a0001c0001t0010g0282others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-10508_379-1049 others(19): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703389 | ||||||
| chr8:101703413
|
G | A | 7 | a0001c0001t0004g0261a0001c0001t0010g0081a0001c0001t0010g0217others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-10517C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703413 | ||||||
| chr8:101703467
|
A | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-10571T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703467 | ||||||
| chr8:101703517
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.379-10621T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703517 | ||||||
| chr8:101703569
|
T | C | 7 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(4): Show | 7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-10673A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703569 | ||||||
| chr8:101703576
|
A | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-10680T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703576 | ||||||
| chr8:101703580
|
A | C | 1 | a0001c0001t0003g0222 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.379-10684T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703580 | ||||||
| chr8:101703703
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-10807C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703703 | ||||||
| chr8:101703858
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.379-10962T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703858 | ||||||
| chr8:101703981
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.379-11085G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703981 | ||||||
| chr8:101704148
|
A | G | 77 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 77 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.379-11252T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704148 | ||||||
| chr8:101704349
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.379-11453G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704349 | ||||||
| chr8:101704531
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.379-11635T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704531 | ||||||
| chr8:101704691
|
C | A | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-11795G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704691 | ||||||
| chr8:101704921
|
AAAAAAAT | A | 3 | a0001c0001t0001g0194a0001c0001t0002g0274a0001c0001t0009g0269 | 3 | HG01167.hp1 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.379-12032_379-1202 others(11): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704921 | ||||||
| chr8:101705211
|
A | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-12315T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705211 | ||||||
| chr8:101705224
|
A | AAAATAAA others(17): Show |
6 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0009g0001others(3): Show | 8 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-12329_379-1232 others(28): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705224 | ||||||
| chr8:101705224
|
A | AAAATAAA others(21): Show |
4 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0139others(1): Show | 4 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-12329_379-1232 others(32): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705224 | ||||||
| chr8:101705224
|
A | AAAATAAA others(25): Show |
3 | a0001c0001t0008g0137a0001c0001t0008g0190a0001c0001t0008g0242 | 3 | NA18981.hp1 NA19068.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.379-12329_379-1232 others(36): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705224 | ||||||
| chr8:101705232
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.379-12336A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705232 | ||||||
| chr8:101705267
|
A | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(8): Show | 11 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-12371T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705267 | ||||||
| chr8:101705340
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.379-12444A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705340 | ||||||
| chr8:101705386
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.379-12490A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705386 | ||||||
| chr8:101705517
|
G | C | 2 | a0001c0001t0003g0114a0001c0001t0003g0115 | 2 | NA18977.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.379-12621C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705517 | ||||||
| chr8:101705525
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.379-12629G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705525 | ||||||
| chr8:101705592
|
G | T | 1 | a0001c0001t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.379-12696C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705592 | ||||||
| chr8:101705654
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.379-12758G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705654 | ||||||
| chr8:101705760
|
A | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-12864T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705760 | ||||||
| chr8:101705823
|
G | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0061 | 2 | HG00738.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.379-12927C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705823 | ||||||
| chr8:101706054
|
G | T | 1 | a0001c0001t0009g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.379-13158C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706054 | ||||||
| chr8:101706134
|
G | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 85 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.378+13118C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706134 | ||||||
| chr8:101706229
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+13023A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706229 | ||||||
| chr8:101706247
|
G | A | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+13005C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706247 | ||||||
| chr8:101706317
|
T | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(54): Show | 58 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.378+12935A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706317 | ||||||
| chr8:101706317
|
T | TA | 7 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(4): Show | 7 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+12934dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706317 | ||||||
| chr8:101706317
|
T | TAAA | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12932_378+1293 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706317 | ||||||
| chr8:101706332
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.378+12920C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706332 | ||||||
| chr8:101706369
|
C | T | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12883G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706369 | ||||||
| chr8:101706380
|
G | A | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12872C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706380 | ||||||
| chr8:101706477
|
A | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12775T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706477 | ||||||
| chr8:101706496
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12756A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706496 | ||||||
| chr8:101706638
|
C | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(180): Show | 187 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.378+12614G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706638 | ||||||
| chr8:101706880
|
AGATAAAT others(5): Show |
A | 73 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 73 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.378+12360_378+1237 others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706880 | ||||||
| chr8:101706922
|
A | G | 93 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 95 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.378+12330T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706922 | ||||||
| chr8:101707035
|
C | T | 85 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 87 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+12217G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707035 | ||||||
| chr8:101707092
|
G | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 87 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+12160C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707092 | ||||||
| chr8:101707344
|
G | A | 7 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(4): Show | 7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+11908C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707344 | ||||||
| chr8:101707405
|
G | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(157): Show | 162 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.378+11847C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707405 | ||||||
| chr8:101707544
|
T | A | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.378+11708A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707544 | ||||||
| chr8:101707606
|
G | C | 1 | a0001c0001t0002g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378+11646C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707606 | ||||||
| chr8:101707614
|
G | A | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11638C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707614 | ||||||
| chr8:101707688
|
A | G | 46 | a0001c0001t0001g0093a0001c0001t0001g0138a0001c0001t0001g0140others(43): Show | 46 | HG00597.hp2 HG00639.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.378+11564T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707688 | ||||||
| chr8:101707692
|
A | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11560T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707692 | ||||||
| chr8:101707736
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02055.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.378+11516G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707736 | ||||||
| chr8:101707746
|
C | T | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11506G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707746 | ||||||
| chr8:101707827
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11425A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707827 | ||||||
| chr8:101707902
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.378+11350T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707902 | ||||||
| chr8:101707903
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.378+11349A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707903 | ||||||
| chr8:101707903
|
TAATA | T | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11345_378+1134 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707903 | ||||||
| chr8:101708011
|
A | G | 4 | a0001c0001t0016g0089a0001c0001t0016g0197a0001c0001t0025g0159others(1): Show | 4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+11241T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708011 | ||||||
| chr8:101708035
|
G | C | 1 | a0001c0001t0002g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378+11217C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708035 | ||||||
| chr8:101708068
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.378+11184C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708068 | ||||||
| chr8:101708125
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11127A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708125 | ||||||
| chr8:101708133
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.378+11119A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708133 | ||||||
| chr8:101708357
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10895A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708357 | ||||||
| chr8:101708654
|
C | CA | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10597dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708654 | ||||||
| chr8:101708658
|
A | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10594T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708658 | ||||||
| chr8:101708674
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.378+10578G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708674 | ||||||
| chr8:101708754
|
T | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+10498A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708754 | ||||||
| chr8:101708812
|
T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(8): Show | 11 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.378+10440A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708812 | ||||||
| chr8:101708841
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.378+10411C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708841 | ||||||
| chr8:101708944
|
A | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10308T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708944 | ||||||
| chr8:101708977
|
C | CT | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10274dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708977 | ||||||
| chr8:101709114
|
G | A | 7 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(4): Show | 7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+10138C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709114 | ||||||
| chr8:101709148
|
C | T | 1 | a0001c0001t0004g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.378+10104G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709148 | ||||||
| chr8:101709196
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.378+10056C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709196 | ||||||
| chr8:101709198
|
C | T | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+10054G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709198 | ||||||
| chr8:101709203
|
G | A | 2 | a0001c0001t0002g0040a0001c0001t0002g0134 | 2 | NA18956.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.378+10049C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709203 | ||||||
| chr8:101709243
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10009A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709243 | ||||||
| chr8:101709362
|
C | T | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9890G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709362 | ||||||
| chr8:101709569
|
C | T | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9683G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709569 | ||||||
| chr8:101709774
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0290 | 2 | HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.378+9478G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709774 | ||||||
| chr8:101709838
|
G | T | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9414C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709838 | ||||||
| chr8:101709881
|
C | CTAA | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9368_378+9370d others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709881 | ||||||
| chr8:101710187
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.378+9065G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710187 | ||||||
| chr8:101710252
|
A | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9000T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710252 | ||||||
| chr8:101710355
|
C | T | 1 | a0001c0001t0002g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.378+8897G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710355 | ||||||
| chr8:101710369
|
G | GTT | 11 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(8): Show | 13 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.378+8881_378+8882d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710369 | ||||||
| chr8:101710389
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0005g0021others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+8863C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710389 | ||||||
| chr8:101710491
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8761A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710491 | ||||||
| chr8:101710620
|
T | C | 1 | a0001c0001t0005g0018 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.378+8632A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710620 | ||||||
| chr8:101710730
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.378+8522C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710730 | ||||||
| chr8:101710764
|
T | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8488A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710764 | ||||||
| chr8:101710974
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.378+8278A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710974 | ||||||
| chr8:101710974
|
T | G | 1 | a0001c0001t0020g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.378+8278A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710974 | ||||||
| chr8:101710975
|
G | A | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8277C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710975 | ||||||
| chr8:101711006
|
A | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8246T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711006 | ||||||
| chr8:101711036
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.378+8216C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711036 | ||||||
| chr8:101711099
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0007g0291 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.378+8153G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711099 | ||||||
| chr8:101711139
|
C | T | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8113G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711139 | ||||||
| chr8:101711141
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.378+8111G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711141 | ||||||
| chr8:101711142
|
C | T | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8110G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711142 | ||||||
| chr8:101711244
|
A | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8008T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711244 | ||||||
| chr8:101711259
|
C | T | 1 | a0001c0001t0019g0046 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.378+7993G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711259 | ||||||
| chr8:101711260
|
GA | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+7991delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711260 | ||||||
| chr8:101711281
|
T | C | 276 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(273): Show | 280 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(277): Show |
intron_variant | MODIFIER | c.378+7971A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711281 | ||||||
| chr8:101711329
|
C | G | 276 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(273): Show | 280 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(277): Show |
intron_variant | MODIFIER | c.378+7923G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711329 | ||||||
| chr8:101711365
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+7887A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711365 | ||||||
| chr8:101711408
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0005g0021others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+7844G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711408 | ||||||
| chr8:101711409
|
G | A | 4 | a0001c0001t0007g0285a0001c0001t0010g0281a0001c0001t0010g0282others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+7843C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711409 | ||||||
| chr8:101711410
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+7842C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711410 | ||||||
| chr8:101711472
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.378+7780G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711472 | ||||||
| chr8:101711507
|
A | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+7745T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711507 | ||||||
| chr8:101711582
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+7670A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711582 | ||||||
| chr8:101711730
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.378+7522C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711730 | ||||||
| chr8:101712004
|
T | C | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.378+7248A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712004 | ||||||
| chr8:101712087
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0010g0281a0001c0001t0010g0282others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+7165G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712087 | ||||||
| chr8:101712237
|
A | G | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+7015T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712237 | ||||||
| chr8:101712244
|
A | G | 1 | a0001c0001t0003g0237 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.378+7008T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712244 | ||||||
| chr8:101712323
|
G | A | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6929C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712323 | ||||||
| chr8:101712415
|
T | C | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6837A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712415 | ||||||
| chr8:101712580
|
T | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(49): Show | 53 | HG00423.hp1 HG00621.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.378+6672A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712580 | ||||||
| chr8:101712587
|
C | CA | 77 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(74): Show | 77 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.378+6664dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | ||||||
| chr8:101712587
|
C | CAA | 18 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0062others(15): Show | 18 | HG00735.hp2 HG01109.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.378+6663_378+6664d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | ||||||
| chr8:101712587
|
C | CAAAAAAA | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+6658_378+6664d others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | ||||||
| chr8:101712587
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0008g0006 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.378+6655_378+6664d others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | ||||||
| chr8:101712587
|
CA | C | 26 | a0001c0001t0001g0268a0001c0001t0002g0009a0001c0001t0002g0102others(23): Show | 26 | HG00597.hp2 HG00639.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.378+6664delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | ||||||
| chr8:101712587
|
CAA | C | 8 | a0001c0001t0002g0274a0001c0001t0004g0261a0001c0001t0010g0081others(5): Show | 8 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+6663_378+6664d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | ||||||
| chr8:101712587
|
CAAAAAAA others(5): Show |
C | 62 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(59): Show | 63 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.378+6653_378+6664d others(14): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | ||||||
| chr8:101712602
|
A | AAG | 12 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(9): Show | 12 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.378+6649_378+6650i others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712602 | ||||||
| chr8:101712692
|
A | G | 5 | a0001c0001t0001g0194a0001c0001t0002g0274a0001c0001t0009g0269others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+6560T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712692 | ||||||
| chr8:101712801
|
G | A | 238 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(235): Show | 240 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(237): Show |
intron_variant | MODIFIER | c.378+6451C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712801 | ||||||
| chr8:101712809
|
T | G | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6443A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712809 | ||||||
| chr8:101712810
|
A | G | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+6442T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712810 | ||||||
| chr8:101712851
|
C | T | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6401G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712851 | ||||||
| chr8:101712969
|
T | C | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6283A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712969 | ||||||
| chr8:101713054
|
G | C | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6198C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713054 | ||||||
| chr8:101713079
|
C | T | 4 | a0001c0001t0004g0261a0001c0001t0011g0036a0001c0001t0011g0110others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+6173G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713079 | ||||||
| chr8:101713089
|
A | AG | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6162_378+6163i others(3): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713089 | ||||||
| chr8:101713293
|
T | C | 5 | a0001c0001t0001g0103a0001c0001t0016g0089a0001c0001t0016g0197others(2): Show | 5 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+5959A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713293 | ||||||
| chr8:101713323
|
A | G | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5929T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713323 | ||||||
| chr8:101713340
|
G | C | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5912C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713340 | ||||||
| chr8:101713353
|
C | G | 35 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0214others(32): Show | 36 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.378+5899G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713353 | ||||||
| chr8:101713454
|
C | CA | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+5797dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713454 | ||||||
| chr8:101713464
|
C | A | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5788G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713464 | ||||||
| chr8:101713493
|
GT | G | 291 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(288): Show | 295 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.378+5758delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713493 | ||||||
| chr8:101713717
|
A | C | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5535T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713717 | ||||||
| chr8:101713756
|
G | A | 43 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0214others(40): Show | 44 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.378+5496C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713756 | ||||||
| chr8:101713782
|
A | G | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5470T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713782 | ||||||
| chr8:101713819
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.378+5433G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713819 | ||||||
| chr8:101713836
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+5416C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713836 | ||||||
| chr8:101713898
|
A | T | 1 | a0001c0001t0004g0084 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.378+5354T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713898 | ||||||
| chr8:101713899
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00609.hp2 HG02071.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+5353C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713899 | ||||||
| chr8:101713899
|
G | C | 1 | a0001c0001t0004g0084 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.378+5353C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713899 | ||||||
| chr8:101713900
|
A | C | 1 | a0001c0001t0004g0084 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.378+5352T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713900 | ||||||
| chr8:101713914
|
T | C | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5338A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713914 | ||||||
| chr8:101714039
|
C | T | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5213G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714039 | ||||||
| chr8:101714075
|
T | C | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5177A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714075 | ||||||
| chr8:101714112
|
G | A | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5140C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714112 | ||||||
| chr8:101714123
|
T | C | 1 | a0001c0001t0007g0284 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.378+5129A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714123 | ||||||
| chr8:101714177
|
A | C | 1 | a0001c0001t0002g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378+5075T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714177 | ||||||
| chr8:101714312
|
G | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(265): Show | 272 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(269): Show |
intron_variant | MODIFIER | c.378+4940C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714312 | ||||||
| chr8:101714508
|
G | C | 1 | a0001c0001t0002g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.378+4744C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714508 | ||||||
| chr8:101714562
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.378+4690A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714562 | ||||||
| chr8:101714699
|
TAAGAACA others(308): Show |
T | 12 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(9): Show | 14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+4238_378+4552d others(2): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714699 | ||||||
| chr8:101714719
|
G | A | 8 | a0001c0001t0001g0185a0001c0001t0004g0261a0001c0001t0010g0081others(5): Show | 8 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+4533C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714719 | ||||||
| chr8:101714859
|
C | T | 8 | a0001c0001t0001g0185a0001c0001t0004g0261a0001c0001t0010g0081others(5): Show | 8 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+4393G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714859 | ||||||
| chr8:101714890
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+4362C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714890 | ||||||
| chr8:101714891
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.378+4361C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714891 | ||||||
| chr8:101714962
|
A | C | 1 | a0001c0001t0023g0052 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.378+4290T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714962 | ||||||
| chr8:101714998
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0107 | 3 | HG01891.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.378+4254G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714998 | ||||||
| chr8:101715003
|
C | CAAAAAAA others(10): Show |
11 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0150others(8): Show | 11 | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.378+4248_378+4249i others(19): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | ||||||
| chr8:101715003
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0001g0032a0001c0001t0001g0264a0001c0001t0007g0286others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+4248_378+4249i others(20): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | ||||||
| chr8:101715003
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0004g0261a0001c0001t0011g0036a0001c0001t0011g0110 | 3 | HG02257.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.378+4248_378+4249i others(21): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | ||||||
| chr8:101715003
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0010g0217a0001c0001t0010g0247a0001c0001t0011g0111 | 3 | HG01074.hp1 HG02109.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.378+4248_378+4249i others(22): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | ||||||
| chr8:101715003
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0010g0081 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.378+4248_378+4249i others(23): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | ||||||
| chr8:101715106
|
C | G | 13 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(10): Show | 15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+4146G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715106 | ||||||
| chr8:101715158
|
C | G | 2 | a0001c0001t0006g0028a0001c0001t0006g0080 | 2 | NA19004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.378+4094G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715158 | ||||||
| chr8:101715206
|
C | T | 7 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0009g0001others(4): Show | 9 | HG02258.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+4046G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715206 | ||||||
| chr8:101715277
|
T | C | 1 | a0001c0001t0006g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.378+3975A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715277 | ||||||
| chr8:101715315
|
T | C | 2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | NA18945.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.378+3937A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715315 | ||||||
| chr8:101715334
|
T | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.378+3918A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715334 | ||||||
| chr8:101715441
|
A | T | 14 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(11): Show | 16 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.378+3811T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715441 | ||||||
| chr8:101715465
|
C | CAACACTG others(3): Show |
14 | a0001c0001t0001g0267a0001c0001t0007g0291a0001c0001t0008g0006others(11): Show | 16 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.378+3786_378+3787i others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715465 | ||||||
| chr8:101715479
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.378+3773A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715479 | ||||||
| chr8:101715818
|
A | G | 5 | a0001c0001t0001g0103a0001c0001t0016g0089a0001c0001t0016g0197others(2): Show | 5 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+3434T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715818 | ||||||
| chr8:101715819
|
C | T | 1 | a0001c0001t0006g0180 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.378+3433G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715819 | ||||||
| chr8:101715878
|
A | T | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0200others(2): Show | 5 | HG01106.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+3374T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715878 | ||||||
| chr8:101716008
|
C | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+3244G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716008 | ||||||
| chr8:101716283
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.378+2969G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716283 | ||||||
| chr8:101716348
|
T | G | 1 | a0001c0001t0001g0012 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.378+2904A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716348 | ||||||
| chr8:101716381
|
A | G | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.378+2871T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716381 | ||||||
| chr8:101716553
|
G | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(239): Show | 244 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.378+2699C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716553 | ||||||
| chr8:101716696
|
G | T | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.378+2556C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716696 | ||||||
| chr8:101716728
|
C | T | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+2524G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716728 | ||||||
| chr8:101716794
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.378+2458C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716794 | ||||||
| chr8:101717175
|
T | C | 48 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(45): Show | 48 | HG00597.hp2 HG01069.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.378+2077A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717175 | ||||||
| chr8:101717247
|
T | C | 49 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(46): Show | 49 | HG00597.hp2 HG01069.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.378+2005A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717247 | ||||||
| chr8:101717701
|
CCAGA | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0187others(6): Show | 9 | HG01109.hp2 HG02074.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+1547_378+1550d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717701 | ||||||
| chr8:101717834
|
T | G | 1 | a0001c0001t0001g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.378+1418A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717834 | ||||||
| chr8:101717992
|
G | A | 277 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(274): Show | 281 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(278): Show |
intron_variant | MODIFIER | c.378+1260C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717992 | ||||||
| chr8:101718069
|
A | C | 20 | a0001c0001t0001g0185a0001c0001t0003g0074a0001c0001t0004g0261others(17): Show | 22 | HG00423.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.378+1183T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718069 | ||||||
| chr8:101718178
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.378+1074C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718178 | ||||||
| chr8:101718225
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.378+1027G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718225 | ||||||
| chr8:101718287
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.378+965G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718287 | ||||||
| chr8:101718846
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(4): Show | 7 | HG01109.hp2 HG02074.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+406A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718846 | ||||||
| chr8:101719136
|
T | A | 30 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0142others(27): Show | 30 | HG00597.hp2 HG01515.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.378+116A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101719136 | ||||||
| chr8:101719246
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.378+6T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101719246 | ||||||
| chr8:101719823
|
AAGAT | A | 3 | a0001c0001t0016g0197a0001c0001t0025g0159a0001c0001t0026g0158 | 3 | HG01069.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-179_-19-176del others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719823 | ||||||
| chr8:101719906
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-19-258G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719906 | ||||||
| chr8:101719912
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-19-264C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719912 | ||||||
| chr8:101719924
|
C | T | 66 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(63): Show | 66 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-19-276G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719924 | ||||||
| chr8:101719925
|
G | A | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-277C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719925 | ||||||
| chr8:101720020
|
A | G | 1 | a0001c0001t0005g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-372T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720020 | ||||||
| chr8:101720021
|
A | C | 1 | a0001c0001t0005g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-373T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720021 | ||||||
| chr8:101720465
|
G | T | 36 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(33): Show | 38 | HG00423.hp2 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-19-817C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720465 | ||||||
| chr8:101720485
|
A | C | 1 | a0001c0001t0020g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-837T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720485 | ||||||
| chr8:101720540
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0083 | 2 | HG01257.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-19-892A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720540 | ||||||
| chr8:101720578
|
C | A | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-930G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720578 | ||||||
| chr8:101720619
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-19-971A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720619 | ||||||
| chr8:101720875
|
T | C | 1 | a0001c0001t0006g0183 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-19-1227A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720875 | ||||||
| chr8:101721064
|
G | A | 1 | a0001c0001t0004g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-19-1416C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721064 | ||||||
| chr8:101721120
|
A | G | 4 | a0001c0001t0001g0283a0001c0001t0007g0284a0001c0001t0007g0286others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-1472T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721120 | ||||||
| chr8:101721168
|
GA | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(210): Show | 217 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.-19-1521delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721168 | ||||||
| chr8:101721168
|
GAA | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.-19-1522_-19-1521d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721168 | ||||||
| chr8:101721363
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-19-1715G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721363 | ||||||
| chr8:101721541
|
G | A | 1 | a0001c0001t0004g0243 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19-1893C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721541 | ||||||
| chr8:101721635
|
C | T | 7 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(4): Show | 7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-1987G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721635 | ||||||
| chr8:101721636
|
G | A | 1 | a0001c0001t0011g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-1988C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721636 | ||||||
| chr8:101721852
|
G | A | 7 | a0001c0001t0004g0261a0001c0001t0010g0081a0001c0001t0010g0217others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2204C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721852 | ||||||
| chr8:101721854
|
C | CTT | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 NA18966.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-2208_-19-2207d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721854 | ||||||
| chr8:101721854
|
CT | C | 73 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0100others(70): Show | 74 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.-19-2207delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721854 | ||||||
| chr8:101721903
|
G | A | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-2255C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721903 | ||||||
| chr8:101722007
|
A | T | 7 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(4): Show | 7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-2359T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722007 | ||||||
| chr8:101722147
|
C | A | 1 | a0001c0001t0005g0249 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19-2499G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722147 | ||||||
| chr8:101722200
|
A | G | 7 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(4): Show | 7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-2552T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722200 | ||||||
| chr8:101722213
|
G | A | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-2565C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722213 | ||||||
| chr8:101722293
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-2645A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722293 | ||||||
| chr8:101722427
|
G | A | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-2779C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722427 | ||||||
| chr8:101722451
|
T | C | 1 | a0001c0001t0020g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-2803A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722451 | ||||||
| chr8:101722670
|
G | A | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-3022C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722670 | ||||||
| chr8:101722839
|
G | T | 12 | a0001c0001t0003g0074a0001c0001t0004g0261a0001c0001t0009g0001others(9): Show | 14 | HG00639.hp2 HG01069.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-3191C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722839 | ||||||
| chr8:101722876
|
T | A | 15 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0238others(12): Show | 15 | HG00544.hp1 HG01099.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19-3228A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722876 | ||||||
| chr8:101723071
|
G | C | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-3423C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723071 | ||||||
| chr8:101723157
|
A | G | 222 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(219): Show | 226 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.-19-3509T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723157 | ||||||
| chr8:101723177
|
G | A | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-3529C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723177 | ||||||
| chr8:101723189
|
CCAGT | C | 6 | a0001c0001t0001g0150a0001c0001t0001g0264a0001c0001t0001g0283others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-3545_-19-3542d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723189 | ||||||
| chr8:101723335
|
T | C | 4 | a0001c0001t0001g0103a0001c0001t0016g0197a0001c0001t0025g0159others(1): Show | 4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-3687A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723335 | ||||||
| chr8:101723714
|
AT | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0005g0021others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-4067delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723714 | ||||||
| chr8:101723896
|
TTTG | T | 16 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0093others(13): Show | 16 | HG00544.hp1 HG01099.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-4251_-19-4249d others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723896 | ||||||
| chr8:101723984
|
G | T | 17 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0041others(14): Show | 17 | HG00738.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19-4336C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723984 | ||||||
| chr8:101724011
|
C | T | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-4363G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724011 | ||||||
| chr8:101724064
|
C | T | 4 | a0001c0001t0001g0103a0001c0001t0016g0197a0001c0001t0025g0159others(1): Show | 4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-4416G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724064 | ||||||
| chr8:101724190
|
TCA | T | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-4544_-19-4543d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724190 | ||||||
| chr8:101724369
|
C | A | 15 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0041others(12): Show | 15 | HG00738.hp1 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-4721G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724369 | ||||||
| chr8:101724491
|
T | C | 8 | a0001c0001t0003g0074a0001c0001t0004g0261a0001c0001t0010g0081others(5): Show | 8 | HG00639.hp2 HG01069.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-4843A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724491 | ||||||
| chr8:101724765
|
AG | A | 4 | a0001c0001t0004g0261a0001c0001t0011g0036a0001c0001t0011g0110others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-5118delC | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724765 | ||||||
| chr8:101724785
|
G | A | 46 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0185others(43): Show | 47 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-19-5137C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724785 | ||||||
| chr8:101724866
|
A | G | 6 | a0001c0001t0001g0150a0001c0001t0001g0264a0001c0001t0001g0283others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5218T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724866 | ||||||
| chr8:101724868
|
C | G | 1 | a0001c0001t0012g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19-5220G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724868 | ||||||
| chr8:101724969
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0004g0292 | 2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-19-5321G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724969 | ||||||
| chr8:101725059
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19-5411A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725059 | ||||||
| chr8:101725112
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-19-5464G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725112 | ||||||
| chr8:101725144
|
A | T | 18 | a0001c0001t0003g0074a0001c0001t0004g0261a0001c0001t0008g0006others(15): Show | 20 | HG00423.hp2 HG00639.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-5496T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725144 | ||||||
| chr8:101725200
|
G | C | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5552C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725200 | ||||||
| chr8:101725341
|
G | A | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5693C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725341 | ||||||
| chr8:101725368
|
G | T | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5720C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725368 | ||||||
| chr8:101725501
|
T | C | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5853A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725501 | ||||||
| chr8:101725563
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-5915T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725563 | ||||||
| chr8:101725798
|
G | A | 12 | a0001c0001t0001g0194a0001c0001t0001g0257a0001c0001t0001g0267others(9): Show | 14 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19-6150C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725798 | ||||||
| chr8:101725850
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-19-6202A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725850 | ||||||
| chr8:101725858
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-19-6210A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725858 | ||||||
| chr8:101725910
|
T | G | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-6262A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725910 | ||||||
| chr8:101725999
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(149): Show | 154 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-19-6351C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725999 | ||||||
| chr8:101726144
|
T | C | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-6496A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726144 | ||||||
| chr8:101726440
|
A | G | 285 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(282): Show | 289 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(286): Show |
intron_variant | MODIFIER | c.-19-6792T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726440 | ||||||
| chr8:101726451
|
G | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0116 | 2 | NA18970.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-19-6803C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726451 | ||||||
| chr8:101726632
|
T | C | 1 | a0001c0001t0003g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19-6984A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726632 | ||||||
| chr8:101726678
|
A | G | 48 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0185others(45): Show | 51 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.-19-7030T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726678 | ||||||
| chr8:101726724
|
G | A | 1 | a0001c0001t0002g0113 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-19-7076C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726724 | ||||||
| chr8:101726736
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0009g0269 | 2 | HG01167.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-19-7088G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726736 | ||||||
| chr8:101726998
|
C | T | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-7350G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726998 | ||||||
| chr8:101727336
|
C | G | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-7688G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727336 | ||||||
| chr8:101727390
|
A | C | 45 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0185others(42): Show | 46 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19-7742T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727390 | ||||||
| chr8:101727490
|
G | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(75): Show | 79 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-19-7842C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727490 | ||||||
| chr8:101727508
|
A | G | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-7860T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727508 | ||||||
| chr8:101727606
|
G | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(65): Show | 69 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-19-7958C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727606 | ||||||
| chr8:101727616
|
G | A | 34 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0214others(31): Show | 35 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-19-7968C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727616 | ||||||
| chr8:101728053
|
G | A | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-8405C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728053 | ||||||
| chr8:101728271
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(64): Show | 68 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-19-8623G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728271 | ||||||
| chr8:101728280
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-19-8632G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728280 | ||||||
| chr8:101728311
|
A | G | 1 | a0001c0001t0005g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-19-8663T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728311 | ||||||
| chr8:101728361
|
C | T | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-8713G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728361 | ||||||
| chr8:101728366
|
C | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(202): Show | 209 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.-19-8718G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728366 | ||||||
| chr8:101728575
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-19-8927G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728575 | ||||||
| chr8:101728591
|
T | C | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-8943A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728591 | ||||||
| chr8:101728611
|
A | G | 210 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(207): Show | 214 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.-19-8963T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728611 | ||||||
| chr8:101728737
|
G | T | 208 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(205): Show | 212 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.-19-9089C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728737 | ||||||
| chr8:101728771
|
A | G | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9123T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728771 | ||||||
| chr8:101728830
|
A | AAAAC | 52 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(49): Show | 53 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.-19-9186_-19-9183d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728830 | ||||||
| chr8:101728855
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19-9207G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728855 | ||||||
| chr8:101728880
|
G | A | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9232C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728880 | ||||||
| chr8:101728932
|
G | A | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9284C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728932 | ||||||
| chr8:101728995
|
G | A | 11 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0142others(8): Show | 11 | HG02738.hp1 NA18940.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19-9347C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728995 | ||||||
| chr8:101729283
|
GA | G | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9636delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729283 | ||||||
| chr8:101729293
|
A | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0005g0021others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-9645T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729293 | ||||||
| chr8:101729462
|
T | C | 1 | a0001c0001t0005g0249 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19-9814A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729462 | ||||||
| chr8:101729530
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(7): Show | 10 | HG01069.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-9882C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729530 | ||||||
| chr8:101729536
|
G | A | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9888C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729536 | ||||||
| chr8:101729578
|
A | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(217): Show | 224 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.-19-9930T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729578 | ||||||
| chr8:101729649
|
C | T | 1 | a0001c0001t0005g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-19-10001G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729649 | ||||||
| chr8:101729707
|
G | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(34): Show | 37 | HG00738.hp1 HG01069.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19-10059C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729707 | ||||||
| chr8:101729765
|
C | T | 6 | a0001c0001t0001g0150a0001c0001t0001g0264a0001c0001t0001g0283others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-10117G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729765 | ||||||
| chr8:101729840
|
A | G | 199 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(196): Show | 201 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.-19-10192T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729840 | ||||||
| chr8:101729914
|
A | C | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-10266T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729914 | ||||||
| chr8:101729961
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0145a0001c0001t0001g0174others(1): Show | 5 | HG01257.hp2 HG01258.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-10313T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729961 | ||||||
| chr8:101729966
|
C | T | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-10318G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729966 | ||||||
| chr8:101729976
|
C | T | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-10328G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729976 | ||||||
| chr8:101730022
|
A | C | 7 | a0001c0001t0001g0008a0001c0001t0008g0006a0001c0001t0008g0091others(4): Show | 7 | HG00423.hp2 HG00597.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-10374T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730022 | ||||||
| chr8:101730093
|
A | G | 2 | a0001c0001t0002g0088a0001c0001t0002g0177 | 2 | HG00423.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-19-10445T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730093 | ||||||
| chr8:101730142
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(223): Show | 230 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.-19-10494A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730142 | ||||||
| chr8:101730165
|
A | G | 46 | a0001c0001t0001g0008a0001c0001t0001g0138a0001c0001t0001g0140others(43): Show | 48 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-19-10517T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730165 | ||||||
| chr8:101730253
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(169): Show | 174 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.-19-10605C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730253 | ||||||
| chr8:101730340
|
G | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(177): Show | 182 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.-19-10692C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730340 | ||||||
| chr8:101730378
|
G | A | 9 | a0001c0001t0001g0227a0001c0001t0002g0182a0001c0001t0004g0078others(6): Show | 9 | HG01167.hp2 HG01515.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-10730C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730378 | ||||||
| chr8:101730402
|
T | C | 187 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(184): Show | 189 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.-19-10754A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730402 | ||||||
| chr8:101730435
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19-10787C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730435 | ||||||
| chr8:101730479
|
C | CA | 31 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0034others(28): Show | 31 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19-10832dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | ||||||
| chr8:101730479
|
C | CAA | 10 | a0001c0001t0001g0228a0001c0001t0001g0293a0001c0001t0002g0067others(7): Show | 10 | HG00544.hp1 HG01074.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-10833_-19-1083 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | ||||||
| chr8:101730479
|
C | CAAA | 95 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(92): Show | 97 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-19-10834_-19-1083 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | ||||||
| chr8:101730479
|
C | CAAAA | 38 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0037others(35): Show | 38 | HG00738.hp1 HG01069.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-19-10835_-19-1083 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | ||||||
| chr8:101730479
|
C | CAAAAA | 17 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0020others(14): Show | 17 | HG00438.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-10836_-19-1083 others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | ||||||
| chr8:101730479
|
C | CAAAAAA | 6 | a0001c0001t0001g0032a0001c0001t0001g0095a0001c0001t0001g0244others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-10837_-19-1083 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | ||||||
| chr8:101730606
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-10958T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730606 | ||||||
| chr8:101730702
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0008g0006a0001c0001t0008g0091others(4): Show | 7 | HG00423.hp2 HG00597.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-11054T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730702 | ||||||
| chr8:101730738
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19-11090A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730738 | ||||||
| chr8:101730770
|
T | C | 1 | a0001c0001t0002g0193 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-19-11122A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730770 | ||||||
| chr8:101730803
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(128): Show | 133 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-19-11155T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730803 | ||||||
| chr8:101730841
|
G | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(134): Show | 139 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-19-11193C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730841 | ||||||
| chr8:101730889
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(127): Show | 132 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.-19-11241A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730889 | ||||||
| chr8:101730927
|
T | G | 6 | a0001c0001t0001g0150a0001c0001t0001g0264a0001c0001t0001g0283others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-11279A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730927 | ||||||
| chr8:101730956
|
C | T | 6 | a0001c0001t0008g0006a0001c0001t0008g0091a0001c0001t0008g0137others(3): Show | 6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-11308G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730956 | ||||||
| chr8:101731014
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-19-11366A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731014 | ||||||
| chr8:101731053
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0273 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.-19-11405C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731053 | ||||||
| chr8:101731223
|
A | T | 1 | a0001c0001t0002g0215 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-11575T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731223 | ||||||
| chr8:101731260
|
G | A | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-11612C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731260 | ||||||
| chr8:101731280
|
G | A | 55 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0185others(52): Show | 56 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-19-11632C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731280 | ||||||
| chr8:101731281
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-11633C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731281 | ||||||
| chr8:101731549
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0008g0091a0001c0001t0008g0190 | 3 | HG00597.hp1 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-19-11901A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731549 | ||||||
| chr8:101731555
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-11907G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731555 | ||||||
| chr8:101731581
|
T | C | 4 | a0001c0001t0009g0001a0001c0001t0009g0155a0001c0001t0009g0260others(1): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-11933A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731581 | ||||||
| chr8:101731584
|
G | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(110): Show | 115 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-19-11936C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731584 | ||||||
| chr8:101731649
|
G | A | 45 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0185others(42): Show | 46 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19-12001C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731649 | ||||||
| chr8:101731784
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-12136T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731784 | ||||||
| chr8:101731821
|
T | A | 82 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(79): Show | 84 | HG00544.hp1 HG00597.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.-19-12173A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731821 | ||||||
| chr8:101731831
|
C | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0041others(15): Show | 18 | HG00738.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19-12183G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731831 | ||||||
| chr8:101732003
|
T | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(95): Show | 98 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.-19-12355A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732003 | ||||||
| chr8:101732260
|
G | A | 4 | a0001c0001t0003g0128a0001c0001t0003g0165a0001c0001t0003g0166others(1): Show | 4 | HG02071.hp1 NA18945.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-12612C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732260 | ||||||
| chr8:101732392
|
C | T | 8 | a0001c0001t0001g0194a0001c0001t0001g0257a0001c0001t0001g0267others(5): Show | 8 | HG01167.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-12744G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732392 | ||||||
| chr8:101732441
|
T | G | 2 | a0001c0001t0025g0159a0001c0001t0026g0158 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-12793A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732441 | ||||||
| chr8:101732493
|
G | A | 83 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(80): Show | 85 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.-19-12845C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732493 | ||||||
| chr8:101732590
|
C | CT | 20 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0057others(17): Show | 20 | HG00544.hp2 HG01106.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-12943dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | ||||||
| chr8:101732590
|
CT | C | 27 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0055others(24): Show | 27 | HG00738.hp2 HG01257.hp1 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19-12943delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | ||||||
| chr8:101732590
|
CTTT | C | 7 | a0001c0001t0003g0074a0001c0001t0004g0261a0001c0001t0010g0217others(4): Show | 7 | HG00639.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-12945_-19-1294 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | ||||||
| chr8:101732590
|
CTTTT | C | 9 | a0001c0001t0001g0008a0001c0001t0007g0030a0001c0001t0008g0006others(6): Show | 9 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-12946_-19-1294 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | ||||||
| chr8:101732590
|
CTTTTT | C | 28 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(25): Show | 28 | HG00423.hp1 HG00597.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19-12947_-19-1294 others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | ||||||
| chr8:101732590
|
CTTTTTT | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(129): Show | 134 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.-19-12948_-19-1294 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | ||||||
| chr8:101732590
|
CTTTTTTT | C | 13 | a0001c0001t0001g0150a0001c0001t0001g0175a0001c0001t0001g0264others(10): Show | 13 | HG00544.hp1 HG01109.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-12949_-19-1294 others(11): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | ||||||
| chr8:101732590
|
CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0035a0001c0001t0006g0028a0001c0001t0006g0080others(11): Show | 16 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-12950_-19-1294 others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | ||||||
| chr8:101732627
|
A | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(134): Show | 138 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.-19-12979T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732627 | ||||||
| chr8:101732756
|
G | A | 20 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0264others(17): Show | 22 | HG00544.hp1 HG01109.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-13108C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732756 | ||||||
| chr8:101732762
|
C | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0107 | 3 | HG01891.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-19-13114G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732762 | ||||||
| chr8:101732814
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-13166C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732814 | ||||||
| chr8:101732970
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | NA18971.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-19-13322A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732970 | ||||||
| chr8:101732971
|
C | A | 10 | a0001c0001t0001g0035a0001c0001t0006g0028a0001c0001t0006g0080others(7): Show | 10 | HG00544.hp1 HG02074.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-13323G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732971 | ||||||
| chr8:101733063
|
C | T | 75 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(72): Show | 77 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-19-13415G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733063 | ||||||
| chr8:101733067
|
C | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0005g0021others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-13419G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733067 | ||||||
| chr8:101733116
|
T | C | 2 | a0001c0001t0025g0159a0001c0001t0026g0158 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-13468A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733116 | ||||||
| chr8:101733123
|
G | C | 81 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(78): Show | 81 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-19-13475C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733123 | ||||||
| chr8:101733193
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(100): Show | 105 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-19-13545G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733193 | ||||||
| chr8:101733194
|
G | A | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(36): Show | 39 | HG00738.hp1 HG01069.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-19-13546C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733194 | ||||||
| chr8:101733551
|
CT | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(100): Show | 105 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-19-13904delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733551 | ||||||
| chr8:101733574
|
G | A | 10 | a0001c0001t0001g0035a0001c0001t0006g0028a0001c0001t0006g0080others(7): Show | 10 | HG00544.hp1 HG02074.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-13926C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733574 | ||||||
| chr8:101733699
|
T | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(207): Show | 212 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.-19-14051A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733699 | ||||||
| chr8:101733724
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-14076G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733724 | ||||||
| chr8:101733825
|
C | G | 1 | a0001c0001t0002g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-19-14177G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733825 | ||||||
| chr8:101733856
|
T | G | 2 | a0001c0001t0003g0205a0001c0001t0003g0212 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-19-14208A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733856 | ||||||
| chr8:101733907
|
G | A | 2 | a0001c0001t0025g0159a0001c0001t0026g0158 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-14259C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733907 | ||||||
| chr8:101733911
|
T | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(102): Show | 107 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-19-14263A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733911 | ||||||
| chr8:101733988
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0290 | 2 | HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-19-14340G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733988 | ||||||
| chr8:101733995
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(99): Show | 104 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-19-14347G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733995 | ||||||
| chr8:101734026
|
C | A | 1 | a0001c0001t0002g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19-14378G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734026 | ||||||
| chr8:101734079
|
T | C | 1 | a0001c0001t0008g0242 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-19-14431A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734079 | ||||||
| chr8:101734091
|
A | C | 8 | a0001c0001t0001g0008a0001c0001t0008g0006a0001c0001t0008g0091others(5): Show | 8 | HG00423.hp2 HG00597.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-14443T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734091 | ||||||
| chr8:101734108
|
G | A | 2 | a0001c0001t0005g0018a0001c0001t0005g0022 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-19-14460C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734108 | ||||||
| chr8:101734208
|
C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(204): Show | 211 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.-19-14560G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734208 | ||||||
| chr8:101734484
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19-14836A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734484 | ||||||
| chr8:101734496
|
C | A | 1 | a0001c0001t0002g0295 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-19-14848G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734496 | ||||||
| chr8:101734944
|
G | A | 196 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(193): Show | 198 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.-19-15296C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734944 | ||||||
| chr8:101735166
|
C | T | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(41): Show | 46 | HG00597.hp2 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19-15518G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735166 | ||||||
| chr8:101735269
|
T | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(88): Show | 94 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-19-15621A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735269 | ||||||
| chr8:101735385
|
G | A | 66 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(63): Show | 68 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.-19-15737C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735385 | ||||||
| chr8:101735430
|
C | T | 2 | a0001c0001t0003g0128a0001c0001t0003g0226 | 2 | HG02071.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.-19-15782G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735430 | ||||||
| chr8:101735475
|
CCT | C | 4 | a0001c0001t0001g0283a0001c0001t0007g0284a0001c0001t0007g0286others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-15829_-19-1582 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735475 | ||||||
| chr8:101735503
|
C | A | 2 | a0001c0001t0001g0194a0001c0001t0009g0269 | 2 | HG01167.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-19-15855G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735503 | ||||||
| chr8:101735580
|
A | C | 1 | a0001c0001t0020g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-15932T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735580 | ||||||
| chr8:101735611
|
C | T | 98 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0031others(95): Show | 99 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.-19-15963G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735611 | ||||||
| chr8:101735653
|
A | T | 1 | a0001c0001t0004g0084 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-19-16005T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735653 | ||||||
| chr8:101735660
|
G | A | 16 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0079others(13): Show | 16 | HG00544.hp1 HG01952.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-16012C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735660 | ||||||
| chr8:101735801
|
T | C | 2 | a0001c0001t0010g0081a0001c0001t0010g0247 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-19-16153A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735801 | ||||||
| chr8:101735831
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-19-16183A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735831 | ||||||
| chr8:101736002
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 178 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-19-16354A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736002 | ||||||
| chr8:101736090
|
G | A | 2 | a0001c0001t0011g0110a0001c0001t0011g0111 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-19-16442C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736090 | ||||||
| chr8:101736202
|
T | C | 5 | a0001c0001t0001g0162a0001c0001t0002g0182a0001c0001t0005g0007others(2): Show | 5 | HG02056.hp2 HG03669.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-16554A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736202 | ||||||
| chr8:101736222
|
C | G | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-16574G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736222 | ||||||
| chr8:101736417
|
A | G | 1 | a0001c0001t0007g0285 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-16769T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736417 | ||||||
| chr8:101736528
|
C | A | 1 | a0001c0001t0005g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-16880G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736528 | ||||||
| chr8:101736582
|
G | A | 11 | a0001c0001t0001g0187a0001c0001t0005g0265a0001c0001t0005g0271others(8): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19-16934C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736582 | ||||||
| chr8:101736583
|
A | G | 2 | a0001c0001t0005g0275a0001c0001t0007g0030 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-19-16935T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736583 | ||||||
| chr8:101736714
|
C | T | 2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | NA18945.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.-19-17066G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736714 | ||||||
| chr8:101736751
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-17103C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736751 | ||||||
| chr8:101736855
|
C | T | 7 | a0001c0001t0001g0248a0001c0001t0001g0253a0001c0001t0004g0254others(4): Show | 7 | HG01074.hp1 HG01515.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-17207G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736855 | ||||||
| chr8:101737018
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-19-17370C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737018 | ||||||
| chr8:101737171
|
T | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0039others(55): Show | 59 | HG00621.hp1 HG00738.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.-19-17523A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737171 | ||||||
| chr8:101737180
|
G | A | 145 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(142): Show | 146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-19-17532C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737180 | ||||||
| chr8:101737340
|
C | A | 173 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(170): Show | 176 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.-19-17692G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737340 | ||||||
| chr8:101737376
|
T | A | 3 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0002g0160 | 3 | HG01081.hp1 HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-19-17728A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737376 | ||||||
| chr8:101737454
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-17806A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737454 | ||||||
| chr8:101737500
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-19-17852A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737500 | ||||||
| chr8:101737542
|
C | T | 149 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-19-17894G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737542 | ||||||
| chr8:101737558
|
G | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(196): Show | 203 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.-19-17910C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737558 | ||||||
| chr8:101737804
|
T | C | 150 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-19-18156A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737804 | ||||||
| chr8:101738163
|
T | C | 165 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(162): Show | 168 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.-19-18515A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738163 | ||||||
| chr8:101738266
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0107others(27): Show | 31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-18618C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738266 | ||||||
| chr8:101738281
|
T | C | 1 | a0001c0001t0002g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-19-18633A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738281 | ||||||
| chr8:101738320
|
G | C | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-19-18672C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738320 | ||||||
| chr8:101738369
|
C | T | 16 | a0001c0001t0001g0248a0001c0001t0001g0253a0001c0001t0001g0257others(13): Show | 18 | HG01074.hp1 HG01109.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19-18721G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738369 | ||||||
| chr8:101738519
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0107others(27): Show | 31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-18871C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738519 | ||||||
| chr8:101738552
|
C | CA | 6 | a0001c0001t0001g0210a0001c0001t0002g0005a0001c0001t0002g0161others(3): Show | 6 | HG01981.hp2 HG02273.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-18905dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738552 | ||||||
| chr8:101738552
|
CAA | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(55): Show | 59 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.-19-18906_-19-1890 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738552 | ||||||
| chr8:101738552
|
CAAAA | C | 22 | a0001c0001t0001g0073a0001c0001t0001g0093a0001c0001t0001g0187others(19): Show | 22 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-18908_-19-1890 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738552 | ||||||
| chr8:101738552
|
CAAAAA | C | 159 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-19-18909_-19-1890 others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738552 | ||||||
| chr8:101738562
|
A | T | 1 | a0001c0001t0009g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-19-18914T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738562 | ||||||
| chr8:101738636
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-18988G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738636 | ||||||
| chr8:101738637
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0015g0108 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-18989C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738637 | ||||||
| chr8:101738799
|
C | T | 2 | a0001c0001t0003g0230a0001c0001t0006g0229 | 2 | NA18950.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-19-19151G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738799 | ||||||
| chr8:101739240
|
A | T | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-19592T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739240 | ||||||
| chr8:101739261
|
T | C | 200 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(197): Show | 203 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.-19-19613A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739261 | ||||||
| chr8:101739277
|
C | A | 7 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0293others(4): Show | 7 | HG00738.hp1 HG01192.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-19629G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739277 | ||||||
| chr8:101739377
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-19-19729C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739377 | ||||||
| chr8:101739381
|
A | G | 1 | a0001c0001t0018g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19-19733T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739381 | ||||||
| chr8:101739499
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0280 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19-19851C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739499 | ||||||
| chr8:101739526
|
T | C | 2 | a0001c0001t0014g0251a0001c0001t0014g0252 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-19878A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739526 | ||||||
| chr8:101739652
|
G | GA | 85 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0087others(82): Show | 88 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.-19-20005dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739652 | ||||||
| chr8:101739729
|
C | G | 6 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0005g0064others(3): Show | 6 | HG01346.hp1 HG01433.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-20081G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739729 | ||||||
| chr8:101739778
|
T | C | 9 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-20130A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739778 | ||||||
| chr8:101739866
|
A | G | 7 | a0001c0001t0001g0087a0001c0001t0001g0238a0001c0001t0001g0239others(4): Show | 7 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-20218T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739866 | ||||||
| chr8:101739935
|
C | A | 7 | a0001c0001t0001g0087a0001c0001t0001g0238a0001c0001t0001g0239others(4): Show | 7 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-20287G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739935 | ||||||
| chr8:101739954
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-19-20306G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739954 | ||||||
| chr8:101739956
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-19-20308A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739956 | ||||||
| chr8:101740069
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-20421A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740069 | ||||||
| chr8:101740180
|
C | A | 1 | a0001c0001t0009g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-19-20532G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740180 | ||||||
| chr8:101740188
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-19-20540C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740188 | ||||||
| chr8:101740306
|
G | T | 1 | a0001c0001t0003g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-19-20658C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740306 | ||||||
| chr8:101740307
|
A | T | 1 | a0001c0001t0003g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-19-20659T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740307 | ||||||
| chr8:101740325
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-19-20677T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740325 | ||||||
| chr8:101740355
|
C | A | 1 | a0001c0001t0005g0141 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-19-20707G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740355 | ||||||
| chr8:101740725
|
A | G | 15 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(12): Show | 15 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-21077T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740725 | ||||||
| chr8:101740871
|
C | T | 2 | a0001c0001t0011g0110a0001c0001t0011g0111 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-19-21223G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740871 | ||||||
| chr8:101741112
|
C | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-21464G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741112 | ||||||
| chr8:101741151
|
C | G | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-21503G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741151 | ||||||
| chr8:101741151
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-21503G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741151 | ||||||
| chr8:101741165
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-19-21517G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741165 | ||||||
| chr8:101741181
|
A | T | 1 | a0001c0001t0007g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-21533T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741181 | ||||||
| chr8:101741182
|
C | T | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-21534G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741182 | ||||||
| chr8:101741354
|
C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(222): Show | 229 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.-19-21706G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741354 | ||||||
| chr8:101741375
|
C | A | 1 | a0001c0001t0003g0231 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-19-21727G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741375 | ||||||
| chr8:101741472
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-19-21824C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741472 | ||||||
| chr8:101741634
|
GA | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-19-21987delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741634 | ||||||
| chr8:101741634
|
GAA | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0039others(76): Show | 82 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.-19-21988_-19-2198 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741634 | ||||||
| chr8:101741637
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-19-21989T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741637 | ||||||
| chr8:101741678
|
G | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0093a0001c0001t0001g0228others(12): Show | 15 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-22030C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741678 | ||||||
| chr8:101741725
|
G | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-19-22077C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741725 | ||||||
| chr8:101741763
|
C | CA | 7 | a0001c0001t0001g0031a0001c0001t0001g0196a0001c0001t0001g0210others(4): Show | 7 | HG01069.hp2 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-22116dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | ||||||
| chr8:101741763
|
CA | C | 127 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0032others(124): Show | 128 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-19-22116delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | ||||||
| chr8:101741763
|
CAA | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0062a0001c0001t0001g0142others(5): Show | 8 | HG00735.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-22117_-19-2211 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | ||||||
| chr8:101741763
|
CAAAAAAA | C | 13 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(10): Show | 13 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-22122_-19-2211 others(11): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | ||||||
| chr8:101741763
|
CAAAAAAA others(1): Show |
C | 62 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(59): Show | 65 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.-19-22123_-19-2211 others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | ||||||
| chr8:101741895
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0004g0156others(1): Show | 4 | HG00738.hp2 HG02622.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-22247G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741895 | ||||||
| chr8:101741923
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0076a0001c0001t0001g0280others(1): Show | 4 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-22275G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741923 | ||||||
| chr8:101741936
|
C | CA | 140 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-22289dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741936 | ||||||
| chr8:101741936
|
CA | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(53): Show | 59 | HG00621.hp1 HG00735.hp1 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.-19-22289delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741936 | ||||||
| chr8:101741936
|
CAA | C | 27 | a0001c0001t0001g0020a0001c0001t0001g0093a0001c0001t0001g0187others(24): Show | 27 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19-22290_-19-2228 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741936 | ||||||
| chr8:101741954
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0004g0104 | 2 | NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-19-22306C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741954 | ||||||
| chr8:101741955
|
A | G | 1 | a0001c0001t0004g0104 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-19-22307T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741955 | ||||||
| chr8:101741959
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0004g0104 | 2 | NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-19-22311C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741959 | ||||||
| chr8:101741959
|
G | GAA | 143 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-22313_-19-2231 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741959 | ||||||
| chr8:101741959
|
GA | G | 16 | a0001c0001t0001g0020a0001c0001t0001g0093a0001c0001t0001g0228others(13): Show | 16 | HG01346.hp1 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-22312delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741959 | ||||||
| chr8:101741996
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-22348C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741996 | ||||||
| chr8:101742089
|
T | A | 1 | a0001c0001t0025g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19-22441A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742089 | ||||||
| chr8:101742090
|
G | GA | 19 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(16): Show | 19 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19-22443dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742090 | ||||||
| chr8:101742090
|
GA | G | 144 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-19-22443delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742090 | ||||||
| chr8:101742135
|
C | A | 2 | a0001c0001t0005g0167a0001c0001t0006g0004 | 2 | HG02027.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-19-22487G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742135 | ||||||
| chr8:101742230
|
GA | G | 144 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-19-22583delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742230 | ||||||
| chr8:101742238
|
A | G | 1 | a0001c0001t0022g0266 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-19-22590T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742238 | ||||||
| chr8:101742256
|
G | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-19-22608C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742256 | ||||||
| chr8:101742358
|
TTC | T | 14 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(11): Show | 14 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-22712_-19-2271 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742358 | ||||||
| chr8:101742420
|
T | G | 1 | a0001c0001t0003g0114 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-19-22772A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742420 | ||||||
| chr8:101742510
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-22862T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742510 | ||||||
| chr8:101742577
|
T | C | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-22929A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742577 | ||||||
| chr8:101742646
|
C | A | 142 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(139): Show | 143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-19-22998G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742646 | ||||||
| chr8:101742664
|
A | AT | 9 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-23017dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742664 | ||||||
| chr8:101742694
|
G | A | 160 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(157): Show | 161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.-19-23046C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742694 | ||||||
| chr8:101742932
|
T | C | 17 | a0001c0001t0001g0020a0001c0001t0001g0093a0001c0001t0001g0228others(14): Show | 17 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19-23284A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742932 | ||||||
| chr8:101742995
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-23347T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742995 | ||||||
| chr8:101743031
|
C | T | 161 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(158): Show | 162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-19-23383G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743031 | ||||||
| chr8:101743267
|
A | G | 1 | a0001c0001t0005g0271 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19-23619T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743267 | ||||||
| chr8:101743282
|
CA | C | 144 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-19-23635delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743282 | ||||||
| chr8:101743378
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-19-23730T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743378 | ||||||
| chr8:101743412
|
C | T | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-23764G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743412 | ||||||
| chr8:101743413
|
A | G | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-23765T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743413 | ||||||
| chr8:101743758
|
G | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-19-24110C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743758 | ||||||
| chr8:101743870
|
T | C | 1 | a0001c0001t0015g0108 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19-24222A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743870 | ||||||
| chr8:101744122
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-19-24474G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744122 | ||||||
| chr8:101744140
|
A | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-24492T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744140 | ||||||
| chr8:101744374
|
A | G | 20 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(17): Show | 22 | HG01109.hp2 HG01891.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-24726T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744374 | ||||||
| chr8:101744462
|
G | T | 146 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-19-24814C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744462 | ||||||
| chr8:101744623
|
A | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-19-24975T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744623 | ||||||
| chr8:101744636
|
A | G | 3 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294 | 3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-24988T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744636 | ||||||
| chr8:101744658
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-19-25010T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744658 | ||||||
| chr8:101744679
|
G | A | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0008g0189others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-25031C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744679 | ||||||
| chr8:101744784
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-25136T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744784 | ||||||
| chr8:101744791
|
A | T | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-19-25143T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744791 | ||||||
| chr8:101744833
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-19-25185C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744833 | ||||||
| chr8:101745126
|
T | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0196a0001c0001t0001g0244others(2): Show | 5 | HG01069.hp2 HG01243.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-25478A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745126 | ||||||
| chr8:101745341
|
G | A | 15 | a0001c0001t0001g0020a0001c0001t0001g0093a0001c0001t0001g0228others(12): Show | 15 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-25693C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745341 | ||||||
| chr8:101745385
|
T | A | 143 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-25737A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745385 | ||||||
| chr8:101745466
|
G | C | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-25818C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745466 | ||||||
| chr8:101745540
|
C | T | 180 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(177): Show | 183 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.-19-25892G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745540 | ||||||
| chr8:101745615
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(39): Show | 43 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-19-25967G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745615 | ||||||
| chr8:101745668
|
G | C | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0008g0189others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-26020C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745668 | ||||||
| chr8:101745727
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-19-26079T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745727 | ||||||
| chr8:101745754
|
C | T | 1 | a0001c0001t0006g0153 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-26106G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745754 | ||||||
| chr8:101745835
|
C | G | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0008g0189others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-26187G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745835 | ||||||
| chr8:101745868
|
T | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-26220A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745868 | ||||||
| chr8:101746302
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-19-26654G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746302 | ||||||
| chr8:101746334
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0002g0040others(1): Show | 4 | NA18956.hp1 NA18956.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-26686C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746334 | ||||||
| chr8:101746335
|
C | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0002g0040others(1): Show | 4 | NA18956.hp1 NA18956.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-26687G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746335 | ||||||
| chr8:101746377
|
A | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-19-26729T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746377 | ||||||
| chr8:101746451
|
CAT | C | 41 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(38): Show | 43 | HG01109.hp2 HG01346.hp1 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.-19-26805_-19-2680 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746451 | ||||||
| chr8:101746507
|
T | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | NA18940.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-19-26859A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746507 | ||||||
| chr8:101746704
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0148a0001c0001t0019g0046 | 3 | HG03239.hp2 NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-19-27056C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746704 | ||||||
| chr8:101746741
|
T | C | 2 | a0001c0001t0002g0102a0001c0001t0004g0078 | 2 | HG00639.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-19-27093A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746741 | ||||||
| chr8:101746782
|
A | G | 3 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0002g0186 | 3 | NA18952.hp1 NA18986.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-19-27134T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746782 | ||||||
| chr8:101746816
|
A | T | 140 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-27168T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746816 | ||||||
| chr8:101747002
|
A | G | 140 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-27354T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747002 | ||||||
| chr8:101747003
|
TTA | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-27357_-19-2735 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747003 | ||||||
| chr8:101747047
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-19-27399A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747047 | ||||||
| chr8:101747055
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0145a0001c0001t0002g0002 | 4 | NA18747.hp2 NA18944.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-27407T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747055 | ||||||
| chr8:101747159
|
A | C | 141 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 142 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-19-27511T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747159 | ||||||
| chr8:101747193
|
TCTC | T | 140 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-27548_-19-2754 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747193 | ||||||
| chr8:101747208
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-19-27560A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747208 | ||||||
| chr8:101747446
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-27798C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747446 | ||||||
| chr8:101747468
|
G | C | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0008g0189others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-27820C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747468 | ||||||
| chr8:101747501
|
C | T | 26 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(23): Show | 28 | HG01109.hp2 HG01346.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19-27853G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747501 | ||||||
| chr8:101747718
|
A | AT | 13 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 13 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-28071dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747718 | ||||||
| chr8:101747718
|
AT | A | 6 | a0001c0001t0001g0077a0001c0001t0002g0213a0001c0001t0009g0269others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-28071delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747718 | ||||||
| chr8:101747718
|
ATT | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-28072_-19-2807 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747718 | ||||||
| chr8:101747809
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(29): Show | 33 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19-28161G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747809 | ||||||
| chr8:101747907
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0015g0108 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-28259C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747907 | ||||||
| chr8:101747916
|
C | T | 2 | a0001c0001t0014g0251a0001c0001t0014g0252 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-28268G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747916 | ||||||
| chr8:101748030
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0015g0108 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-28382T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748030 | ||||||
| chr8:101748214
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(28): Show | 32 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-19-28566A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748214 | ||||||
| chr8:101748257
|
T | G | 145 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(142): Show | 146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-19-28609A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748257 | ||||||
| chr8:101748330
|
C | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(31): Show | 35 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-19-28682G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748330 | ||||||
| chr8:101748421
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0007g0168 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-28773G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748421 | ||||||
| chr8:101748609
|
C | T | 1 | a0001c0001t0008g0006 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-19-28961G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748609 | ||||||
| chr8:101748907
|
G | A | 228 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(225): Show | 232 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.-19-29259C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748907 | ||||||
| chr8:101748946
|
G | A | 9 | a0001c0001t0001g0116a0001c0001t0001g0120a0001c0001t0002g0117others(6): Show | 9 | HG01081.hp1 HG01952.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-29298C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748946 | ||||||
| chr8:101748947
|
C | G | 1 | a0001c0001t0004g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-19-29299G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748947 | ||||||
| chr8:101748999
|
C | T | 3 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294 | 3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-29351G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748999 | ||||||
| chr8:101749104
|
G | A | 228 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(225): Show | 232 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.-19-29456C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749104 | ||||||
| chr8:101749142
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-19-29494T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749142 | ||||||
| chr8:101749171
|
C | T | 1 | a0001c0001t0008g0242 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-19-29523G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749171 | ||||||
| chr8:101749387
|
A | T | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-29739T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749387 | ||||||
| chr8:101749494
|
G | T | 10 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0195others(7): Show | 10 | HG01074.hp2 HG01261.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-29846C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749494 | ||||||
| chr8:101749591
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-29943C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749591 | ||||||
| chr8:101749603
|
C | T | 217 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(214): Show | 221 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.-19-29955G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749603 | ||||||
| chr8:101749754
|
G | A | 166 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-19-30106C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749754 | ||||||
| chr8:101749846
|
G | A | 163 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(160): Show | 164 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.-19-30198C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749846 | ||||||
| chr8:101750130
|
A | G | 166 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-19-30482T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750130 | ||||||
| chr8:101750222
|
TC | T | 216 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(213): Show | 220 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.-19-30575delG | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750222 | ||||||
| chr8:101750229
|
C | G | 3 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294 | 3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-30581G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750229 | ||||||
| chr8:101750299
|
A | G | 1 | a0001c0001t0023g0052 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-19-30651T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750299 | ||||||
| chr8:101750308
|
A | T | 169 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(166): Show | 170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-19-30660T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750308 | ||||||
| chr8:101750568
|
A | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(223): Show | 230 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.-19-30920T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750568 | ||||||
| chr8:101750661
|
T | C | 1 | a0001c0001t0005g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-31013A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750661 | ||||||
| chr8:101750696
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-31048G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750696 | ||||||
| chr8:101750785
|
A | G | 172 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(169): Show | 173 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19-31137T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750785 | ||||||
| chr8:101750786
|
C | A | 172 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(169): Show | 173 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19-31138G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750786 | ||||||
| chr8:101750891
|
T | C | 3 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294 | 3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-31243A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750891 | ||||||
| chr8:101750906
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19-31258C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750906 | ||||||
| chr8:101750953
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0280a0001c0001t0007g0030 | 3 | HG02257.hp1 HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19-31305C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750953 | ||||||
| chr8:101751011
|
C | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG02080.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-19-31363G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751011 | ||||||
| chr8:101751113
|
G | A | 1 | a0001c0001t0016g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19-31465C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751113 | ||||||
| chr8:101751126
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-31478G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751126 | ||||||
| chr8:101751174
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-31526G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751174 | ||||||
| chr8:101751277
|
C | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-31629G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751277 | ||||||
| chr8:101751319
|
G | A | 1 | a0001c0001t0008g0132 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-19-31671C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751319 | ||||||
| chr8:101751345
|
G | A | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-31697C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751345 | ||||||
| chr8:101751415
|
C | A | 3 | a0001c0001t0001g0234a0001c0001t0002g0236a0001c0001t0004g0235 | 3 | HG02083.hp1 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-19-31767G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751415 | ||||||
| chr8:101751416
|
T | A | 3 | a0001c0001t0001g0234a0001c0001t0002g0236a0001c0001t0004g0235 | 3 | HG02083.hp1 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-19-31768A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751416 | ||||||
| chr8:101751475
|
G | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(17): Show | 21 | HG00621.hp1 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-19-31827C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751475 | ||||||
| chr8:101751515
|
G | T | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-31867C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751515 | ||||||
| chr8:101751603
|
G | A | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-31955C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751603 | ||||||
| chr8:101751773
|
C | T | 141 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 142 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-19-32125G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751773 | ||||||
| chr8:101751775
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-32127C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751775 | ||||||
| chr8:101751780
|
T | A | 143 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-32132A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751780 | ||||||
| chr8:101751782
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-19-32134G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751782 | ||||||
| chr8:101751805
|
T | G | 1 | a0001c0001t0001g0220 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-19-32157A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751805 | ||||||
| chr8:101751810
|
G | T | 11 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(8): Show | 11 | HG02083.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-32162C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751810 | ||||||
| chr8:101751829
|
T | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-19-32181A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751829 | ||||||
| chr8:101751889
|
C | T | 4 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-32241G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751889 | ||||||
| chr8:101751906
|
C | G | 141 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 142 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-19-32258G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751906 | ||||||
| chr8:101751907
|
G | A | 2 | a0001c0001t0025g0159a0001c0001t0026g0158 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-32259C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751907 | ||||||
| chr8:101752185
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-32537A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752185 | ||||||
| chr8:101752257
|
T | C | 147 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-19-32609A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752257 | ||||||
| chr8:101752358
|
A | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-19-32710T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752358 | ||||||
| chr8:101752526
|
T | G | 1 | a0001c0001t0001g0157 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-19-32878A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752526 | ||||||
| chr8:101752629
|
A | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0032others(33): Show | 37 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.-19-32981T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752629 | ||||||
| chr8:101752718
|
C | T | 221 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(218): Show | 225 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.-19-33070G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752718 | ||||||
| chr8:101752832
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-33184G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752832 | ||||||
| chr8:101752957
|
T | C | 1 | a0001c0001t0012g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19-33309A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752957 | ||||||
| chr8:101752957
|
T | TGTATTTT others(319): Show |
7 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(4): Show | 7 | HG02647.hp2 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-33310_-19-3330 others(330): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752957 | ||||||
| chr8:101752957
|
T | TGTATTTT others(321): Show |
1 | a0001c0001t0005g0271 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19-33310_-19-3330 others(332): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752957 | ||||||
| chr8:101753075
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-19-33427C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753075 | ||||||
| chr8:101753402
|
A | T | 2 | a0001c0001t0001g0253a0001c0001t0004g0255 | 2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-19-33754T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753402 | ||||||
| chr8:101753654
|
T | C | 143 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-34006A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753654 | ||||||
| chr8:101753720
|
G | A | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-19-34072C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753720 | ||||||
| chr8:101753724
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-34076C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753724 | ||||||
| chr8:101753777
|
G | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-34129C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753777 | ||||||
| chr8:101753948
|
T | A | 151 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.-19-34300A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753948 | ||||||
| chr8:101753956
|
T | A | 2 | a0001c0001t0004g0094a0001c0001t0004g0104 | 2 | NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-19-34308A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753956 | ||||||
| chr8:101754014
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(180): Show | 185 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.-19-34366C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754014 | ||||||
| chr8:101754076
|
T | C | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-34428A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754076 | ||||||
| chr8:101754144
|
G | C | 1 | a0001c0001t0004g0078 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-19-34496C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754144 | ||||||
| chr8:101754237
|
C | G | 9 | a0001c0001t0001g0257a0001c0001t0001g0264a0001c0001t0004g0261others(6): Show | 11 | HG01109.hp2 HG02258.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-34589G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754237 | ||||||
| chr8:101754285
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-34637T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754285 | ||||||
| chr8:101754309
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-19-34661G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754309 | ||||||
| chr8:101754311
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-34663A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754311 | ||||||
| chr8:101754311
|
T | G | 141 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 142 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-19-34663A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754311 | ||||||
| chr8:101754337
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-19-34689C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754337 | ||||||
| chr8:101754369
|
G | A | 143 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-34721C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754369 | ||||||
| chr8:101754499
|
C | A | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19-34851G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754499 | ||||||
| chr8:101754521
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-19-34873C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754521 | ||||||
| chr8:101754776
|
A | G | 153 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(150): Show | 154 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-19-35128T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754776 | ||||||
| chr8:101754799
|
G | A | 189 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(186): Show | 191 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.-19-35151C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754799 | ||||||
| chr8:101754866
|
GAATA | G | 3 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294 | 3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-35222_-19-3521 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754866 | ||||||
| chr8:101754870
|
A | G | 1 | a0001c0001t0007g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-35222T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754870 | ||||||
| chr8:101755005
|
C | G | 1 | a0001c0001t0021g0122 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-19-35357G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755005 | ||||||
| chr8:101755024
|
T | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(185): Show | 190 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.-19-35376A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755024 | ||||||
| chr8:101755161
|
T | C | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-35513A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755161 | ||||||
| chr8:101755251
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-35603C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755251 | ||||||
| chr8:101755324
|
ATTCCCGT | A | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-20+35531_-20+3553 others(11): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755324 | ||||||
| chr8:101755377
|
T | C | 1 | a0001c0001t0004g0224 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-20+35485A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755377 | ||||||
| chr8:101755429
|
T | C | 148 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.-20+35433A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755429 | ||||||
| chr8:101755435
|
C | T | 148 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.-20+35427G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755435 | ||||||
| chr8:101755490
|
C | A | 177 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 180 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-20+35372G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755490 | ||||||
| chr8:101755612
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-20+35250C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755612 | ||||||
| chr8:101755652
|
T | C | 1 | a0001c0001t0008g0190 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-20+35210A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755652 | ||||||
| chr8:101755770
|
G | T | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+35092C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755770 | ||||||
| chr8:101755836
|
T | C | 1 | a0001c0001t0006g0181 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-20+35026A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755836 | ||||||
| chr8:101755839
|
T | G | 150 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-20+35023A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755839 | ||||||
| chr8:101756039
|
G | A | 1 | a0001c0001t0002g0193 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-20+34823C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756039 | ||||||
| chr8:101756078
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-20+34784G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756078 | ||||||
| chr8:101756084
|
CT | C | 181 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(178): Show | 183 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.-20+34777delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756084 | ||||||
| chr8:101756160
|
G | A | 147 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-20+34702C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756160 | ||||||
| chr8:101756246
|
T | G | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+34616A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756246 | ||||||
| chr8:101756481
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-20+34381C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756481 | ||||||
| chr8:101756561
|
C | T | 6 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0002g0049others(3): Show | 6 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+34301G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756561 | ||||||
| chr8:101756611
|
A | C | 1 | a0001c0001t0005g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+34251T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756611 | ||||||
| chr8:101756750
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-20+34112G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756750 | ||||||
| chr8:101757102
|
C | G | 1 | a0001c0001t0002g0170 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-20+33760G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757102 | ||||||
| chr8:101757156
|
C | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(192): Show | 197 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.-20+33706G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757156 | ||||||
| chr8:101757279
|
T | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(213): Show | 220 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.-20+33583A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757279 | ||||||
| chr8:101757302
|
C | G | 2 | a0001c0001t0008g0189a0001c0001t0008g0190 | 2 | HG02523.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-20+33560G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757302 | ||||||
| chr8:101757321
|
T | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+33541A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757321 | ||||||
| chr8:101757372
|
C | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0039others(27): Show | 31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+33490G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757372 | ||||||
| chr8:101757381
|
G | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(37): Show | 41 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20+33481C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757381 | ||||||
| chr8:101757531
|
T | C | 143 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-20+33331A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757531 | ||||||
| chr8:101757609
|
T | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(188): Show | 193 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.-20+33253A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757609 | ||||||
| chr8:101757679
|
T | A | 143 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-20+33183A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757679 | ||||||
| chr8:101757715
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+33147A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757715 | ||||||
| chr8:101757726
|
C | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(38): Show | 42 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.-20+33136G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757726 | ||||||
| chr8:101757874
|
A | C | 3 | a0001c0001t0001g0234a0001c0001t0002g0236a0001c0001t0004g0235 | 3 | HG02083.hp1 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-20+32988T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757874 | ||||||
| chr8:101757877
|
G | A | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(4): Show | 7 | HG01069.hp1 HG01952.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+32985C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757877 | ||||||
| chr8:101757878
|
AG | A | 7 | a0001c0001t0001g0039a0001c0001t0002g0177a0001c0001t0006g0178others(4): Show | 7 | HG00621.hp1 HG02083.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+32983delC | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757878 | ||||||
| chr8:101757899
|
T | A | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-20+32963A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757899 | ||||||
| chr8:101757910
|
A | G | 2 | a0001c0001t0008g0189a0001c0001t0008g0190 | 2 | HG02523.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-20+32952T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757910 | ||||||
| chr8:101758127
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0015g0108 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-20+32735A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758127 | ||||||
| chr8:101758236
|
T | C | 27 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(24): Show | 29 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.-20+32626A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758236 | ||||||
| chr8:101758308
|
C | T | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+32554G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758308 | ||||||
| chr8:101758378
|
C | T | 1 | a0001c0001t0004g0243 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+32484G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758378 | ||||||
| chr8:101758466
|
A | G | 2 | a0001c0001t0004g0169a0001c0001t0007g0168 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-20+32396T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758466 | ||||||
| chr8:101758625
|
C | T | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-20+32237G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758625 | ||||||
| chr8:101758674
|
C | T | 3 | a0001c0001t0011g0036a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-20+32188G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758674 | ||||||
| chr8:101758750
|
C | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(3): Show | 6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+32112G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758750 | ||||||
| chr8:101758826
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(223): Show | 230 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.-20+32036A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758826 | ||||||
| chr8:101758831
|
T | C | 150 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-20+32031A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758831 | ||||||
| chr8:101758833
|
C | T | 1 | a0001c0001t0003g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-20+32029G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758833 | ||||||
| chr8:101758833
|
CT | C | 147 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-20+32028delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758833 | ||||||
| chr8:101758938
|
A | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+31924T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758938 | ||||||
| chr8:101758939
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+31923G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758939 | ||||||
| chr8:101759001
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-20+31861G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759001 | ||||||
| chr8:101759012
|
T | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0174others(26): Show | 30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+31850A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759012 | ||||||
| chr8:101759065
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+31797C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759065 | ||||||
| chr8:101759100
|
C | A | 1 | a0001c0001t0007g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-20+31762G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759100 | ||||||
| chr8:101759170
|
G | A | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+31692C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759170 | ||||||
| chr8:101759340
|
CA | C | 7 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0002g0118others(4): Show | 7 | HG01081.hp1 HG01952.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+31521delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759340 | ||||||
| chr8:101759455
|
T | C | 1 | a0001c0001t0005g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+31407A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759455 | ||||||
| chr8:101759637
|
G | A | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0008g0189others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+31225C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759637 | ||||||
| chr8:101759743
|
G | C | 2 | a0001c0001t0001g0184a0001c0001t0002g0163 | 2 | HG00735.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+31119C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759743 | ||||||
| chr8:101759821
|
G | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0039others(42): Show | 46 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-20+31041C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759821 | ||||||
| chr8:101759828
|
C | G | 12 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(9): Show | 12 | HG00738.hp1 HG01192.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+31034G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759828 | ||||||
| chr8:101759952
|
G | A | 19 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(16): Show | 21 | HG01099.hp1 HG01109.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.-20+30910C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759952 | ||||||
| chr8:101759994
|
C | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0280a0001c0001t0007g0030 | 3 | HG02257.hp1 HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-20+30868G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759994 | ||||||
| chr8:101760207
|
T | A | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+30655A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760207 | ||||||
| chr8:101760558
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-20+30304A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760558 | ||||||
| chr8:101760618
|
T | C | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+30244A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760618 | ||||||
| chr8:101760658
|
A | T | 289 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(286): Show | 293 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.-20+30204T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760658 | ||||||
| chr8:101760729
|
G | C | 2 | a0001c0001t0007g0278a0001c0001t0007g0279 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-20+30133C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760729 | ||||||
| chr8:101760744
|
A | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0162others(27): Show | 31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+30118T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760744 | ||||||
| chr8:101761156
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(3): Show | 6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+29706G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761156 | ||||||
| chr8:101761260
|
C | T | 231 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(228): Show | 235 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(232): Show |
intron_variant | MODIFIER | c.-20+29602G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761260 | ||||||
| chr8:101761492
|
A | G | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+29370T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761492 | ||||||
| chr8:101761501
|
A | G | 1 | a0001c0001t0007g0250 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-20+29361T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761501 | ||||||
| chr8:101761675
|
G | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+29187C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761675 | ||||||
| chr8:101761685
|
T | C | 138 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 139 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-20+29177A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761685 | ||||||
| chr8:101761717
|
T | C | 4 | a0001c0001t0001g0283a0001c0001t0007g0284a0001c0001t0007g0286others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+29145A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761717 | ||||||
| chr8:101761817
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-20+29045C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761817 | ||||||
| chr8:101762157
|
T | C | 1 | a0001c0001t0004g0224 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-20+28705A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762157 | ||||||
| chr8:101762163
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0010g0247 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-20+28699G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762163 | ||||||
| chr8:101762213
|
A | C | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+28649T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762213 | ||||||
| chr8:101762279
|
A | C | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0008g0189others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+28583T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762279 | ||||||
| chr8:101762279
|
A | G | 1 | a0001c0001t0003g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-20+28583T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762279 | ||||||
| chr8:101762295
|
T | C | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+28567A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762295 | ||||||
| chr8:101762352
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(215): Show | 220 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.-20+28510C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762352 | ||||||
| chr8:101762457
|
T | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(3): Show | 6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+28405A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762457 | ||||||
| chr8:101762591
|
C | CT | 9 | a0001c0001t0001g0210a0001c0001t0001g0293a0001c0001t0002g0005others(6): Show | 9 | HG00738.hp1 HG01192.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+28270dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762591 | ||||||
| chr8:101762591
|
CT | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(56): Show | 62 | HG00621.hp1 HG00735.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.-20+28270delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762591 | ||||||
| chr8:101762608
|
T | C | 19 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0253others(16): Show | 21 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-20+28254A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762608 | ||||||
| chr8:101762633
|
G | A | 1 | a0001c0001t0002g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-20+28229C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762633 | ||||||
| chr8:101762718
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-20+28144G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762718 | ||||||
| chr8:101762816
|
C | T | 1 | a0001c0001t0007g0250 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-20+28046G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762816 | ||||||
| chr8:101762822
|
T | C | 1 | a0001c0001t0005g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+28040A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762822 | ||||||
| chr8:101762864
|
G | A | 1 | a0001c0001t0004g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-20+27998C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762864 | ||||||
| chr8:101762948
|
A | G | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+27914T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762948 | ||||||
| chr8:101763124
|
T | C | 1 | a0001c0001t0003g0222 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-20+27738A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763124 | ||||||
| chr8:101763218
|
C | T | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+27644G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763218 | ||||||
| chr8:101763256
|
C | A | 8 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+27606G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763256 | ||||||
| chr8:101763432
|
C | T | 2 | a0001c0001t0002g0121a0001c0001t0008g0132 | 2 | NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-20+27430G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763432 | ||||||
| chr8:101763497
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20+27365A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763497 | ||||||
| chr8:101763506
|
G | T | 6 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0002g0236others(3): Show | 6 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+27356C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763506 | ||||||
| chr8:101763518
|
C | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0008g0189others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+27344G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763518 | ||||||
| chr8:101763630
|
C | T | 35 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 36 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-20+27232G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763630 | ||||||
| chr8:101763732
|
G | T | 1 | a0001c0001t0001g0098 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-20+27130C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763732 | ||||||
| chr8:101763877
|
G | A | 1 | a0001c0001t0007g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20+26985C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763877 | ||||||
| chr8:101763921
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-20+26941G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763921 | ||||||
| chr8:101763952
|
T | TTCTCTCT others(1): Show |
4 | a0001c0001t0001g0264a0001c0001t0004g0263a0001c0001t0013g0258others(1): Show | 4 | HG01109.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26902_-20+2690 others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763952 | ||||||
| chr8:101763952
|
T | TTCTCTCT others(3): Show |
3 | a0001c0001t0001g0253a0001c0001t0004g0255a0001c0001t0004g0256 | 3 | HG01891.hp2 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-20+26900_-20+2690 others(14): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763952 | ||||||
| chr8:101763965
|
T | TC | 3 | a0001c0001t0001g0184a0001c0001t0002g0163a0001c0001t0003g0164 | 3 | HG00735.hp1 HG03491.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+26896dupG | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763965 | ||||||
| chr8:101763966
|
C | CCA | 4 | a0001c0001t0001g0013a0001c0001t0001g0106a0001c0001t0001g0127others(1): Show | 4 | HG02165.hp2 HG04199.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26894_-20+2689 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | ||||||
| chr8:101763966
|
C | CCCTCTCT others(3): Show |
1 | a0001c0001t0002g0186 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-20+26895_-20+2689 others(14): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | ||||||
| chr8:101763966
|
C | CT | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+26895_-20+2689 others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | ||||||
| chr8:101763966
|
C | CTCTCTCT others(5): Show |
5 | a0001c0001t0004g0254a0001c0001t0004g0261a0001c0001t0009g0001others(2): Show | 7 | HG02145.hp1 HG02258.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+26895_-20+2689 others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | ||||||
| chr8:101763966
|
C | CTCTCTCT others(7): Show |
1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+26895_-20+2689 others(18): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | ||||||
| chr8:101763966
|
CCA | C | 6 | a0001c0001t0001g0043a0001c0001t0002g0014a0001c0001t0002g0192others(3): Show | 6 | HG01069.hp2 HG02080.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+26894_-20+2689 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | ||||||
| chr8:101763966
|
CCACA | C | 11 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0042others(8): Show | 12 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20+26892_-20+2689 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | ||||||
| chr8:101763966
|
CCACACA | C | 4 | a0001c0001t0001g0032a0001c0001t0005g0275a0001c0001t0006g0206others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26890_-20+2689 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | ||||||
| chr8:101763967
|
C | CCTCT | 5 | a0001c0001t0001g0162a0001c0001t0003g0165a0001c0001t0003g0166others(2): Show | 5 | HG02027.hp1 HG03669.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+26894_-20+2689 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763967 | ||||||
| chr8:101763967
|
C | CCTCTCT | 18 | a0001c0001t0001g0003a0001c0001t0001g0174a0001c0001t0001g0175others(15): Show | 19 | HG00621.hp1 HG01243.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20+26894_-20+2689 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763967 | ||||||
| chr8:101763967
|
C | T | 4 | a0001c0001t0001g0264a0001c0001t0004g0263a0001c0001t0013g0258others(1): Show | 4 | HG01109.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26895G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763967 | ||||||
| chr8:101763968
|
A | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0162a0001c0001t0001g0174others(24): Show | 28 | HG00621.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-20+26894T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763968 | ||||||
| chr8:101763968
|
A | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0184others(5): Show | 8 | HG00735.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20+26894T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763968 | ||||||
| chr8:101763969
|
C | T | 5 | a0001c0001t0001g0162a0001c0001t0003g0165a0001c0001t0003g0166others(2): Show | 5 | HG02027.hp1 HG03669.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+26893G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763969 | ||||||
| chr8:101763970
|
A | C | 5 | a0001c0001t0001g0162a0001c0001t0003g0165a0001c0001t0003g0166others(2): Show | 5 | HG02027.hp1 HG03669.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+26892T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763970 | ||||||
| chr8:101763970
|
A | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0184others(6): Show | 9 | HG00735.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+26892T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763970 | ||||||
| chr8:101763971
|
C | CT | 3 | a0001c0001t0001g0184a0001c0001t0002g0163a0001c0001t0003g0164 | 3 | HG00735.hp1 HG03491.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+26890_-20+2689 others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763971 | ||||||
| chr8:101763972
|
A | C | 3 | a0001c0001t0001g0184a0001c0001t0002g0163a0001c0001t0003g0164 | 3 | HG00735.hp1 HG03491.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+26890T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763972 | ||||||
| chr8:101763972
|
A | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(3): Show | 6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+26890T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763972 | ||||||
| chr8:101763973
|
CA | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+26888delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763973 | ||||||
| chr8:101763974
|
A | T | 1 | a0001c0001t0005g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+26888T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763974 | ||||||
| chr8:101763976
|
A | T | 1 | a0001c0001t0005g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+26886T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763976 | ||||||
| chr8:101763990
|
ACACACAC others(19): Show |
A | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20+26846_-20+2687 others(30): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763990 | ||||||
| chr8:101763998
|
ACACACAC others(11): Show |
A | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20+26846_-20+2686 others(22): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763998 | ||||||
| chr8:101764000
|
ACACACAC others(9): Show |
A | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-20+26846_-20+2686 others(20): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764000 | ||||||
| chr8:101764002
|
ACACACAC others(7): Show |
A | 5 | a0001c0001t0001g0234a0001c0001t0002g0236a0001c0001t0004g0235others(2): Show | 5 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(18): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764002 | ||||||
| chr8:101764004
|
ACACACAC others(5): Show |
A | 2 | a0001c0001t0001g0187a0001c0001t0019g0046 | 2 | NA18953.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764004 | ||||||
| chr8:101764006
|
ACACACAC others(3): Show |
A | 8 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0048others(5): Show | 8 | HG01081.hp2 HG01257.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(14): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764006 | ||||||
| chr8:101764006
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0148 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-20+26844_-20+2685 others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764006 | ||||||
| chr8:101764008
|
ACACACAC others(1): Show |
A | 30 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0055others(27): Show | 30 | HG00609.hp2 HG01106.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764008 | ||||||
| chr8:101764010
|
ACACACC | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0038others(61): Show | 64 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764010 | ||||||
| chr8:101764012
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-20+26850T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764012 | ||||||
| chr8:101764012
|
ACACC | A | 40 | a0001c0001t0001g0019a0001c0001t0001g0083a0001c0001t0001g0085others(37): Show | 40 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2684 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764012 | ||||||
| chr8:101764012
|
ACACCC | A | 3 | a0001c0001t0001g0010a0001c0001t0008g0137a0001c0001t0014g0252 | 3 | HG06807.hp2 NA18981.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-20+26845_-20+2684 others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764012 | ||||||
| chr8:101764014
|
ACC | A | 44 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0098others(41): Show | 44 | HG00597.hp2 HG00609.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2684 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764014 | ||||||
| chr8:101764014
|
ACCC | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0116a0001c0001t0001g0143others(4): Show | 7 | HG03831.hp2 NA18983.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+26845_-20+2684 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764014 | ||||||
| chr8:101764016
|
C | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0105others(40): Show | 44 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.-20+26846G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764016 | ||||||
| chr8:101764079
|
A | T | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+26783T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764079 | ||||||
| chr8:101764090
|
G | A | 6 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0002g0236others(3): Show | 6 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+26772C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764090 | ||||||
| chr8:101764108
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(3): Show | 6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+26754A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764108 | ||||||
| chr8:101764189
|
A | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+26673T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764189 | ||||||
| chr8:101764200
|
T | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 51 | HG00621.hp1 HG00735.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-20+26662A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764200 | ||||||
| chr8:101764286
|
A | C | 1 | a0001c0001t0001g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+26576T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764286 | ||||||
| chr8:101764297
|
A | G | 7 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0001g0234others(4): Show | 7 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+26565T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764297 | ||||||
| chr8:101764504
|
C | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0008g0189others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26358G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764504 | ||||||
| chr8:101764607
|
T | C | 36 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0093others(33): Show | 38 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.-20+26255A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764607 | ||||||
| chr8:101764691
|
T | C | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26171A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764691 | ||||||
| chr8:101764805
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-20+26057A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764805 | ||||||
| chr8:101765059
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20+25803C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765059 | ||||||
| chr8:101765089
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0006g0151 | 2 | HG00544.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-20+25773G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765089 | ||||||
| chr8:101765115
|
C | T | 8 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+25747G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765115 | ||||||
| chr8:101765200
|
G | T | 1 | a0001c0001t0003g0205 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-20+25662C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765200 | ||||||
| chr8:101765275
|
A | G | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 59 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-20+25587T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765275 | ||||||
| chr8:101765327
|
T | A | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+25535A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765327 | ||||||
| chr8:101765430
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+25432A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765430 | ||||||
| chr8:101765535
|
T | C | 1 | a0001c0001t0003g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-20+25327A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765535 | ||||||
| chr8:101765659
|
G | C | 1 | a0001c0001t0002g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-20+25203C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765659 | ||||||
| chr8:101765728
|
T | G | 8 | a0001c0001t0001g0187a0001c0001t0001g0267a0001c0001t0001g0268others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+25134A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765728 | ||||||
| chr8:101766086
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0002g0040 | 3 | NA18946.hp2 NA18969.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-20+24776G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766086 | ||||||
| chr8:101766372
|
T | TA | 238 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(235): Show | 242 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.-20+24489dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766372 | ||||||
| chr8:101766488
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+24374C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766488 | ||||||
| chr8:101766524
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20+24338A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766524 | ||||||
| chr8:101766754
|
T | A | 6 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0002g0236others(3): Show | 6 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+24108A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766754 | ||||||
| chr8:101766834
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0037others(8): Show | 11 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+24028G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766834 | ||||||
| chr8:101766935
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0174a0001c0001t0001g0175others(27): Show | 31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+23927C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766935 | ||||||
| chr8:101767043
|
T | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0174a0001c0001t0001g0175others(27): Show | 31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+23819A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767043 | ||||||
| chr8:101767054
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-20+23808C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767054 | ||||||
| chr8:101767136
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0017others(3): Show | 6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+23726G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767136 | ||||||
| chr8:101767225
|
T | C | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+23637A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767225 | ||||||
| chr8:101767461
|
A | G | 1 | a0001c0001t0007g0250 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-20+23401T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767461 | ||||||
| chr8:101767729
|
C | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0174a0001c0001t0001g0175others(20): Show | 24 | HG00621.hp1 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.-20+23133G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767729 | ||||||
| chr8:101767882
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-20+22980G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767882 | ||||||
| chr8:101767908
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0280a0001c0001t0005g0275 | 3 | HG02257.hp1 HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-20+22954C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767908 | ||||||
| chr8:101768091
|
G | T | 4 | a0001c0001t0007g0030a0001c0001t0011g0036a0001c0001t0011g0110others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+22771C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768091 | ||||||
| chr8:101768335
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-20+22527T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768335 | ||||||
| chr8:101768389
|
GGGC | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(211): Show | 216 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.-20+22470_-20+2247 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768389 | ||||||
| chr8:101768641
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-20+22221C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768641 | ||||||
| chr8:101768720
|
A | AAC | 33 | a0001c0001t0001g0003a0001c0001t0001g0174a0001c0001t0001g0175others(30): Show | 34 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20+22141_-20+2214 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768720 | ||||||
| chr8:101768723
|
C | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0174a0001c0001t0001g0175others(30): Show | 34 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20+22139G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768723 | ||||||
| chr8:101768723
|
C | CA | 177 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 178 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-20+22138dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768723 | ||||||
| chr8:101769221
|
G | T | 162 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 163 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-20+21641C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769221 | ||||||
| chr8:101769268
|
C | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(233): Show | 240 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.-20+21594G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769268 | ||||||
| chr8:101769402
|
A | G | 6 | a0001c0001t0001g0116a0001c0001t0002g0113a0001c0001t0002g0117others(3): Show | 6 | NA18948.hp2 NA18971.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+21460T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769402 | ||||||
| chr8:101769491
|
C | T | 6 | a0001c0001t0001g0248a0001c0001t0005g0249a0001c0001t0007g0250others(3): Show | 6 | HG01074.hp1 HG01515.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+21371G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769491 | ||||||
| chr8:101769493
|
G | A | 162 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 163 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-20+21369C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769493 | ||||||
| chr8:101769655
|
C | A | 1 | a0001c0001t0001g0105 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-20+21207G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769655 | ||||||
| chr8:101769681
|
C | T | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+21181G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769681 | ||||||
| chr8:101769703
|
T | C | 7 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(4): Show | 7 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+21159A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769703 | ||||||
| chr8:101769876
|
A | G | 2 | a0001c0001t0001g0280a0001c0001t0005g0275 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+20986T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769876 | ||||||
| chr8:101769880
|
T | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 46 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-20+20982A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769880 | ||||||
| chr8:101769948
|
C | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+20914G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769948 | ||||||
| chr8:101769962
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-20+20900G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769962 | ||||||
| chr8:101769984
|
A | G | 1 | a0001c0001t0007g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+20878T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769984 | ||||||
| chr8:101770257
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20+20605T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770257 | ||||||
| chr8:101770312
|
G | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0174a0001c0001t0001g0175others(38): Show | 44 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.-20+20550C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770312 | ||||||
| chr8:101770332
|
T | C | 2 | a0001c0001t0001g0280a0001c0001t0005g0275 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+20530A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770332 | ||||||
| chr8:101770355
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-20+20507A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770355 | ||||||
| chr8:101770539
|
C | T | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+20323G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770539 | ||||||
| chr8:101770589
|
A | G | 159 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.-20+20273T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770589 | ||||||
| chr8:101770876
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-20+19986G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770876 | ||||||
| chr8:101771178
|
G | A | 1 | a0001c0001t0003g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-20+19684C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101771178 | ||||||
| chr8:101771297
|
GT | G | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+19564delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101771297 | ||||||
| chr8:101771946
|
A | C | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+18916T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101771946 | ||||||
| chr8:101772089
|
A | G | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+18773T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772089 | ||||||
| chr8:101772205
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+18657G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772205 | ||||||
| chr8:101772315
|
C | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+18547G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772315 | ||||||
| chr8:101772339
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+18523C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772339 | ||||||
| chr8:101772442
|
A | C | 1 | a0001c0001t0002g0163 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-20+18420T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772442 | ||||||
| chr8:101772552
|
A | G | 11 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0195others(8): Show | 11 | HG00438.hp2 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+18310T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772552 | ||||||
| chr8:101772658
|
A | G | 5 | a0001c0001t0001g0196a0001c0001t0001g0244a0001c0001t0002g0274others(2): Show | 5 | HG01069.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+18204T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772658 | ||||||
| chr8:101773018
|
T | A | 1 | a0001c0001t0018g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-20+17844A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773018 | ||||||
| chr8:101773084
|
G | T | 1 | a0001c0001t0004g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-20+17778C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773084 | ||||||
| chr8:101773310
|
C | T | 1 | a0001c0001t0012g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-20+17552G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773310 | ||||||
| chr8:101773360
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-20+17502A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773360 | ||||||
| chr8:101773809
|
C | T | 1 | a0001c0001t0003g0237 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-20+17053G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773809 | ||||||
| chr8:101773822
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-20+17040C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773822 | ||||||
| chr8:101773832
|
A | C | 7 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0002g0236others(4): Show | 7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+17030T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773832 | ||||||
| chr8:101773999
|
C | T | 7 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0002g0236others(4): Show | 7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+16863G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773999 | ||||||
| chr8:101774103
|
G | C | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+16759C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774103 | ||||||
| chr8:101774189
|
C | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+16673G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774189 | ||||||
| chr8:101774190
|
T | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+16672A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774190 | ||||||
| chr8:101774266
|
T | C | 7 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0002g0236others(4): Show | 7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+16596A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774266 | ||||||
| chr8:101774275
|
G | T | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+16587C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774275 | ||||||
| chr8:101774355
|
A | G | 1 | a0001c0001t0006g0028 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-20+16507T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774355 | ||||||
| chr8:101774459
|
T | C | 1 | a0001c0001t0008g0132 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-20+16403A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774459 | ||||||
| chr8:101774619
|
G | A | 1 | a0001c0001t0002g0186 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-20+16243C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774619 | ||||||
| chr8:101774676
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-20+16186G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774676 | ||||||
| chr8:101774690
|
G | A | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+16172C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774690 | ||||||
| chr8:101774805
|
T | C | 1 | a0001c0001t0003g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-20+16057A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774805 | ||||||
| chr8:101775101
|
C | T | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+15761G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775101 | ||||||
| chr8:101775369
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-20+15493C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775369 | ||||||
| chr8:101775559
|
A | G | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 61 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-20+15303T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775559 | ||||||
| chr8:101775625
|
C | A | 2 | a0001c0001t0001g0107a0001c0001t0015g0108 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-20+15237G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775625 | ||||||
| chr8:101775664
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-20+15198G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775664 | ||||||
| chr8:101775767
|
C | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+15095G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775767 | ||||||
| chr8:101775801
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-20+15061C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775801 | ||||||
| chr8:101775876
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-20+14986T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775876 | ||||||
| chr8:101776058
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-20+14804G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776058 | ||||||
| chr8:101776072
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0162a0001c0001t0001g0174others(28): Show | 32 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-20+14790A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776072 | ||||||
| chr8:101776094
|
T | C | 1 | a0001c0001t0004g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-20+14768A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776094 | ||||||
| chr8:101776186
|
C | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+14676G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776186 | ||||||
| chr8:101776228
|
A | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+14634T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776228 | ||||||
| chr8:101776234
|
C | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(71): Show | 77 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.-20+14628G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776234 | ||||||
| chr8:101776448
|
C | G | 3 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294 | 3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-20+14414G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776448 | ||||||
| chr8:101776457
|
A | AT | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+14404dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776457 | ||||||
| chr8:101776706
|
G | A | 5 | a0001c0001t0002g0026a0001c0001t0002g0134a0001c0001t0003g0135others(2): Show | 5 | NA18956.hp1 NA18974.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+14156C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776706 | ||||||
| chr8:101776812
|
C | G | 1 | a0001c0001t0010g0281 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-20+14050G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776812 | ||||||
| chr8:101776814
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-20+14048A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776814 | ||||||
| chr8:101776851
|
G | A | 8 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0142others(5): Show | 8 | HG02451.hp2 NA18950.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20+14011C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776851 | ||||||
| chr8:101776870
|
A | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+13992T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776870 | ||||||
| chr8:101777032
|
C | A | 7 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0002g0236others(4): Show | 7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+13830G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777032 | ||||||
| chr8:101777044
|
C | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+13818G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777044 | ||||||
| chr8:101777139
|
C | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG02080.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-20+13723G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777139 | ||||||
| chr8:101777304
|
T | C | 2 | a0001c0001t0007g0278a0001c0001t0007g0279 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-20+13558A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777304 | ||||||
| chr8:101777479
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+13383A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777479 | ||||||
| chr8:101777571
|
G | A | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+13291C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777571 | ||||||
| chr8:101777641
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-20+13221C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777641 | ||||||
| chr8:101777762
|
T | C | 73 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(70): Show | 76 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.-20+13100A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777762 | ||||||
| chr8:101777763
|
G | A | 1 | a0001c0001t0004g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-20+13099C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777763 | ||||||
| chr8:101777859
|
T | C | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+13003A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777859 | ||||||
| chr8:101777978
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+12884A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777978 | ||||||
| chr8:101778103
|
C | A | 2 | a0001c0001t0011g0110a0001c0001t0011g0111 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-20+12759G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778103 | ||||||
| chr8:101778144
|
T | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+12718A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778144 | ||||||
| chr8:101778482
|
T | G | 51 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 52 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.-20+12380A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778482 | ||||||
| chr8:101778666
|
G | A | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+12196C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778666 | ||||||
| chr8:101778892
|
A | T | 5 | a0001c0001t0001g0234a0001c0001t0002g0236a0001c0001t0004g0235others(2): Show | 5 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+11970T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778892 | ||||||
| chr8:101779100
|
T | C | 1 | a0001c0001t0010g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-20+11762A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779100 | ||||||
| chr8:101779115
|
A | G | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+11747T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779115 | ||||||
| chr8:101779134
|
C | G | 2 | a0001c0001t0001g0280a0001c0001t0005g0275 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+11728G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779134 | ||||||
| chr8:101779134
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+11728G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779134 | ||||||
| chr8:101779167
|
A | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+11695T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779167 | ||||||
| chr8:101779177
|
A | T | 1 | a0001c0001t0003g0191 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-20+11685T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779177 | ||||||
| chr8:101779238
|
TAATCCAG others(34): Show |
T | 1 | a0001c0001t0002g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-20+11583_-20+1162 others(45): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779238 | ||||||
| chr8:101779388
|
T | C | 2 | a0001c0001t0001g0280a0001c0001t0005g0275 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+11474A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779388 | ||||||
| chr8:101779618
|
G | T | 1 | a0001c0001t0005g0249 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-20+11244C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779618 | ||||||
| chr8:101779739
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-20+11123C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779739 | ||||||
| chr8:101779783
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+11079G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779783 | ||||||
| chr8:101780304
|
A | G | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+10558T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780304 | ||||||
| chr8:101780484
|
G | C | 1 | a0001c0001t0004g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+10378C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780484 | ||||||
| chr8:101780530
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+10332T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780530 | ||||||
| chr8:101780539
|
A | G | 2 | a0001c0001t0008g0189a0001c0001t0008g0190 | 2 | HG02523.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-20+10323T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780539 | ||||||
| chr8:101780592
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+10270T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780592 | ||||||
| chr8:101780690
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-20+10172C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780690 | ||||||
| chr8:101780694
|
A | G | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+10168T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780694 | ||||||
| chr8:101780726
|
C | T | 234 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(231): Show | 238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.-20+10136G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780726 | ||||||
| chr8:101780791
|
T | C | 2 | a0001c0001t0014g0251a0001c0001t0014g0252 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+10071A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780791 | ||||||
| chr8:101780844
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0162a0001c0001t0001g0174others(48): Show | 54 | HG00621.hp1 HG00735.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-20+10018T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780844 | ||||||
| chr8:101780960
|
G | A | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0002g0295others(1): Show | 4 | HG02132.hp2 NA18612.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+9902C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780960 | ||||||
| chr8:101781044
|
G | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+9818C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781044 | ||||||
| chr8:101781183
|
AAT | A | 233 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(230): Show | 237 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.-20+9677_-20+9678d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781183 | ||||||
| chr8:101781257
|
G | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+9605C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781257 | ||||||
| chr8:101781443
|
G | A | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+9419C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781443 | ||||||
| chr8:101781482
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-20+9380G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781482 | ||||||
| chr8:101781661
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-20+9201C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781661 | ||||||
| chr8:101781726
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-20+9136C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781726 | ||||||
| chr8:101781893
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0162a0001c0001t0001g0174others(28): Show | 32 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-20+8969T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781893 | ||||||
| chr8:101781908
|
T | A | 223 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(220): Show | 225 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.-20+8954A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781908 | ||||||
| chr8:101781922
|
A | G | 4 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0007g0278others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+8940T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781922 | ||||||
| chr8:101781961
|
T | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8901A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781961 | ||||||
| chr8:101781995
|
C | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8867G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781995 | ||||||
| chr8:101781997
|
TA | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8864delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781997 | ||||||
| chr8:101782007
|
T | C | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+8855A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782007 | ||||||
| chr8:101782040
|
T | TG | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8821dupC | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782040 | ||||||
| chr8:101782071
|
ATATTG | A | 156 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(153): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.-20+8786_-20+8790d others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782071 | ||||||
| chr8:101782076
|
G | A | 28 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(25): Show | 28 | HG00738.hp1 HG01099.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.-20+8786C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782076 | ||||||
| chr8:101782111
|
T | TATATATT others(10): Show |
9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8750_-20+8751i others(19): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782111 | ||||||
| chr8:101782272
|
C | A | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8590G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782272 | ||||||
| chr8:101782294
|
A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(10): Show | 13 | HG00738.hp1 HG01192.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+8568T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782294 | ||||||
| chr8:101782314
|
C | T | 6 | a0001c0001t0001g0150a0001c0001t0001g0234a0001c0001t0002g0236others(3): Show | 6 | HG02083.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+8548G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782314 | ||||||
| chr8:101782394
|
A | C | 7 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0002g0236others(4): Show | 7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+8468T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782394 | ||||||
| chr8:101782646
|
A | G | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8216T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782646 | ||||||
| chr8:101782847
|
C | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8015G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782847 | ||||||
| chr8:101783035
|
T | C | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+7827A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783035 | ||||||
| chr8:101783044
|
T | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+7818A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783044 | ||||||
| chr8:101783071
|
G | C | 1 | a0001c0001t0001g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-20+7791C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783071 | ||||||
| chr8:101783249
|
G | A | 1 | a0001c0001t0004g0256 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-20+7613C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783249 | ||||||
| chr8:101783451
|
T | G | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+7411A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783451 | ||||||
| chr8:101783688
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-20+7174G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783688 | ||||||
| chr8:101784006
|
T | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6856A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784006 | ||||||
| chr8:101784077
|
A | G | 1 | a0001c0001t0002g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-20+6785T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784077 | ||||||
| chr8:101784164
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0283a0001c0001t0007g0284others(6): Show | 9 | HG02559.hp1 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+6698G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784164 | ||||||
| chr8:101784342
|
A | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+6520T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784342 | ||||||
| chr8:101784344
|
T | C | 3 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294 | 3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-20+6518A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784344 | ||||||
| chr8:101784392
|
G | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0174a0001c0001t0001g0175others(55): Show | 61 | HG00621.hp1 HG00735.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.-20+6470C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784392 | ||||||
| chr8:101784534
|
T | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6328A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784534 | ||||||
| chr8:101784627
|
A | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6235T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784627 | ||||||
| chr8:101784651
|
T | A | 30 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(27): Show | 30 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.-20+6211A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784651 | ||||||
| chr8:101784790
|
A | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+6072T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784790 | ||||||
| chr8:101784825
|
A | G | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6037T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784825 | ||||||
| chr8:101784851
|
G | C | 2 | a0001c0001t0001g0152a0001c0001t0006g0151 | 2 | HG00544.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-20+6011C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784851 | ||||||
| chr8:101784862
|
G | T | 5 | a0001c0001t0001g0234a0001c0001t0002g0236a0001c0001t0004g0235others(2): Show | 5 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+6000C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784862 | ||||||
| chr8:101784934
|
CA | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0280a0001c0001t0001g0289others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+5927delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784934 | ||||||
| chr8:101784971
|
A | C | 1 | a0001c0001t0005g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-20+5891T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784971 | ||||||
| chr8:101785000
|
A | G | 8 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0005g0265others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+5862T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785000 | ||||||
| chr8:101785091
|
A | G | 2 | a0001c0001t0025g0159a0001c0001t0026g0158 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-20+5771T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785091 | ||||||
| chr8:101785263
|
C | A | 1 | a0001c0001t0006g0153 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-20+5599G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785263 | ||||||
| chr8:101785402
|
T | G | 4 | a0001c0001t0001g0233a0001c0001t0003g0230a0001c0001t0003g0231others(1): Show | 4 | HG02074.hp2 NA18950.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+5460A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785402 | ||||||
| chr8:101785489
|
C | T | 149 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-20+5373G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785489 | ||||||
| chr8:101785513
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+5349A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785513 | ||||||
| chr8:101785515
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0009g0155 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-20+5347C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785515 | ||||||
| chr8:101785541
|
G | T | 15 | a0001c0001t0001g0280a0001c0001t0001g0283a0001c0001t0001g0289others(12): Show | 15 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+5321C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785541 | ||||||
| chr8:101785585
|
A | T | 13 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(10): Show | 15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+5277T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785585 | ||||||
| chr8:101785675
|
A | G | 14 | a0001c0001t0001g0283a0001c0001t0001g0289a0001c0001t0001g0290others(11): Show | 14 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+5187T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785675 | ||||||
| chr8:101785702
|
C | T | 14 | a0001c0001t0001g0283a0001c0001t0001g0289a0001c0001t0001g0290others(11): Show | 14 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+5160G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785702 | ||||||
| chr8:101785752
|
A | C | 2 | a0001c0001t0001g0248a0001c0001t0010g0247 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-20+5110T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785752 | ||||||
| chr8:101785769
|
G | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0162a0001c0001t0001g0174others(27): Show | 31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+5093C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785769 | ||||||
| chr8:101785869
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20+4993T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785869 | ||||||
| chr8:101786126
|
A | G | 14 | a0001c0001t0001g0283a0001c0001t0001g0289a0001c0001t0001g0290others(11): Show | 14 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+4736T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786126 | ||||||
| chr8:101786337
|
G | A | 150 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-20+4525C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786337 | ||||||
| chr8:101786351
|
T | G | 1 | a0001c0001t0004g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-20+4511A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786351 | ||||||
| chr8:101786486
|
C | A | 1 | a0001c0001t0001g0233 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20+4376G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786486 | ||||||
| chr8:101786511
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-20+4351C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786511 | ||||||
| chr8:101786527
|
T | C | 7 | a0001c0001t0001g0234a0001c0001t0002g0236a0001c0001t0004g0235others(4): Show | 7 | HG02083.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+4335A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786527 | ||||||
| chr8:101786548
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-20+4314A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786548 | ||||||
| chr8:101786663
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+4199T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786663 | ||||||
| chr8:101786701
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+4161C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786701 | ||||||
| chr8:101786987
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-20+3875G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786987 | ||||||
| chr8:101787098
|
A | G | 12 | a0001c0001t0001g0283a0001c0001t0001g0293a0001c0001t0004g0292others(9): Show | 12 | HG00738.hp1 HG01192.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+3764T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787098 | ||||||
| chr8:101787266
|
C | T | 151 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.-20+3596G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787266 | ||||||
| chr8:101787341
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20+3521G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787341 | ||||||
| chr8:101787362
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-20+3500G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787362 | ||||||
| chr8:101787396
|
G | A | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+3466C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787396 | ||||||
| chr8:101787526
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20+3336C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787526 | ||||||
| chr8:101787809
|
G | A | 1 | a0001c0001t0004g0243 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+3053C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787809 | ||||||
| chr8:101787909
|
A | C | 1 | a0001c0001t0005g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+2953T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787909 | ||||||
| chr8:101788005
|
T | C | 2 | a0001c0001t0001g0244a0001c0001t0018g0245 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-20+2857A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788005 | ||||||
| chr8:101788074
|
T | A | 12 | a0001c0001t0001g0283a0001c0001t0001g0293a0001c0001t0004g0292others(9): Show | 12 | HG00738.hp1 HG01192.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+2788A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788074 | ||||||
| chr8:101788157
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0004g0254a0001c0001t0004g0255others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+2705G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788157 | ||||||
| chr8:101788164
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+2698C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788164 | ||||||
| chr8:101788231
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+2631G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788231 | ||||||
| chr8:101788252
|
T | C | 12 | a0001c0001t0001g0283a0001c0001t0001g0293a0001c0001t0004g0292others(9): Show | 12 | HG00738.hp1 HG01192.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+2610A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788252 | ||||||
| chr8:101788383
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+2479G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788383 | ||||||
| chr8:101788435
|
T | G | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2427A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788435 | ||||||
| chr8:101788436
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2426A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788436 | ||||||
| chr8:101788437
|
G | T | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2425C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788437 | ||||||
| chr8:101788438
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2424A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788438 | ||||||
| chr8:101788440
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2422C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788440 | ||||||
| chr8:101788443
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2419C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788443 | ||||||
| chr8:101788445
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2417A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788445 | ||||||
| chr8:101788446
|
A | C | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2416T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788446 | ||||||
| chr8:101788447
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2415A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788447 | ||||||
| chr8:101788448
|
C | A | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2414G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788448 | ||||||
| chr8:101788499
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-20+2363A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788499 | ||||||
| chr8:101788622
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+2240G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788622 | ||||||
| chr8:101788838
|
T | A | 1 | a0001c0001t0005g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-20+2024A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788838 | ||||||
| chr8:101788876
|
T | C | 6 | a0001c0001t0001g0248a0001c0001t0005g0249a0001c0001t0007g0250others(3): Show | 6 | HG01074.hp1 HG01515.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+1986A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788876 | ||||||
| chr8:101788939
|
GGTT | G | 21 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0264others(18): Show | 23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-20+1920_-20+1922d others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788939 | ||||||
| chr8:101789005
|
G | C | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-20+1857C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789005 | ||||||
| chr8:101789135
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG00423.hp2 HG00597.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+1727T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789135 | ||||||
| chr8:101789135
|
A | T | 14 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0280others(11): Show | 14 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+1727T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789135 | ||||||
| chr8:101789142
|
A | C | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1720T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789142 | ||||||
| chr8:101789348
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+1514T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789348 | ||||||
| chr8:101789497
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20+1365A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789497 | ||||||
| chr8:101789525
|
C | T | 1 | a0001c0001t0005g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+1337G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789525 | ||||||
| chr8:101789567
|
A | G | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1295T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789567 | ||||||
| chr8:101789809
|
G | C | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1053C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789809 | ||||||
| chr8:101789812
|
G | A | 14 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0280others(11): Show | 14 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+1050C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789812 | ||||||
| chr8:101789859
|
A | G | 1 | a0001c0001t0002g0005 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-20+1003T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789859 | ||||||
| chr8:101789905
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+957C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789905 | ||||||
| chr8:101789921
|
T | C | 4 | a0001c0001t0001g0293a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+941A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789921 | ||||||
| chr8:101789978
|
A | ATCCAGAG others(21): Show |
1 | a0001c0001t0006g0004 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-20+856_-20+883dup others(28): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789978 | ||||||
| chr8:101790601
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-20+261C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101790601 | ||||||
| chr8:101790725
|
T | C | 1 | a0001c0001t0003g0296 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-20+137A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101790725 |