Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 28513 |
|---|---|
| ensemblid | ENSG00000071991.9 |
| hgncid | 1758 |
| symbol | CDH19 |
| name | cadherin 19 |
| refseq_nuc | NM_021153.4 |
| refseq_prot | NP_066976.1 |
| ensembl_nuc | ENST00000262150.7 |
| ensembl_prot | ENSP00000262150.2 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 66501083 |
| end | 66604090 |
| strand | - |
| ver | v1.2 |
| region | chr18:66501083-66604090 |
| region5000 | chr18:66496083-66609090 |
| regionname0 | CDH19_chr18_66501083_66604090 |
| regionname5000 | CDH19_chr18_66496083_66609090 |
| 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 | 772 | 307 | 71 | 42 | 155 | 11 | 26 | 126 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0002 | 0/0 | 772 | 20 | 0 | 14 | 1 | 1 | 4 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0003 | 0/0 | 772 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0004 | 0/0 | 772 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0005 | 0/0 | 772 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0006 | 0/0 | 772 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0007 | 0/0 | 772 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0008 | 0/0 | 291 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0009 | 0/0 | 772 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0010 | 0/0 | 772 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0011 | 0/0 | 772 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0012 | 0/0 | 772 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0013 | 0/0 | 772 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0014 | 0/0 | 772 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0015 | 0/0 | 772 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0016 | 0/0 | 772 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0017 | 0/0 | 772 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2319 | 188 | 62 | 24 | 88 | 3 | 10 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0002 | 0/1 | 2319 | 78 | 4 | 11 | 44 | 5 | 13 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0003 | 0/0 | 2319 | 32 | 5 | 3 | 21 | 0 | 3 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0004 | 0/0 | 2319 | 20 | 0 | 14 | 1 | 1 | 4 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0005 | 0/0 | 2319 | 6 | 6 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0006 | 0/0 | 2319 | 4 | 3 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0007 | 0/0 | 2319 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0008 | 0/0 | 2319 | 3 | 0 | 1 | 0 | 2 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0009 | 0/0 | 2319 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0010 | 0/0 | 2319 | 2 | 0 | 1 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0011 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0012 | 0/0 | 2319 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0013 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0014 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0015 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0016 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0017 | 0/0 | 1880 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0018 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0019 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0020 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0021 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0022 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0023 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0024 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| c0025 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| 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 | 0/1 | 3979 | 69 | 3 | 12 | 35 | 7 | 11 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0002 | 0/0 | 3981 | 59 | 9 | 9 | 36 | 1 | 4 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0003 | 0/0 | 3981 | 55 | 6 | 11 | 32 | 3 | 3 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0004 | 0/0 | 3980 | 48 | 9 | 7 | 25 | 1 | 6 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0005 | 0/0 | 3983 | 14 | 0 | 9 | 1 | 1 | 3 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0006 | 0/0 | 3982 | 10 | 9 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0007 | 0/0 | 3980 | 10 | 2 | 0 | 8 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0008 | 0/0 | 3978 | 9 | 0 | 1 | 6 | 0 | 2 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0009 | 0/0 | 3979 | 8 | 8 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0010 | 0/0 | 3981 | 7 | 7 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0011 | 0/0 | 3974 | 7 | 7 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0012 | 0/0 | 3982 | 5 | 0 | 4 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0013 | 0/0 | 3979 | 5 | 3 | 0 | 2 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0014 | 0/0 | 3979 | 4 | 1 | 2 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0015 | 0/0 | 3982 | 3 | 2 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0016 | 0/0 | 3981 | 3 | 0 | 0 | 3 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0017 | 0/0 | 3980 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0018 | 0/0 | 3980 | 3 | 0 | 0 | 3 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0019 | 0/0 | 3980 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0020 | 0/0 | 3977 | 2 | 2 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0021 | 0/0 | 3981 | 2 | 1 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0022 | 0/0 | 3979 | 2 | 2 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0023 | 1/0 | 3979 | 2 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0024 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0025 | 0/0 | 3977 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0026 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0027 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0028 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0029 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0030 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0031 | 0/0 | 3981 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0032 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0033 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0034 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0035 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0036 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0037 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0038 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0039 | 0/0 | 3980 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0040 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0041 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0042 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0043 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| t0044 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2319 | 188 | 62 | 24 | 88 | 3 | 10 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0002 | 0/1 | 2319 | 78 | 4 | 11 | 44 | 5 | 13 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0003 | 0/0 | 2319 | 32 | 5 | 3 | 21 | 0 | 3 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0008 | 0/0 | 2319 | 3 | 0 | 1 | 0 | 2 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0010 | 0/0 | 2319 | 2 | 0 | 1 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0011 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0014 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0018 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0024 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0002c0004 | 0/0 | 2319 | 20 | 0 | 14 | 1 | 1 | 4 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0003c0005 | 0/0 | 2319 | 6 | 6 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0004c0006 | 0/0 | 2319 | 4 | 3 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0005c0009 | 0/0 | 2319 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0006c0007 | 0/0 | 2319 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0007c0012 | 0/0 | 2319 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0008c0017 | 0/0 | 1880 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0009c0019 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0010c0020 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0011c0021 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0012c0022 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0013c0016 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0014c0023 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0015c0015 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0016c0025 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0017c0013 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 6299 | 53 | 7 | 6 | 35 | 1 | 4 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0003 | 0/0 | 6299 | 49 | 6 | 9 | 30 | 1 | 3 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0004 | 0/0 | 6298 | 17 | 4 | 4 | 5 | 1 | 3 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0006 | 0/0 | 6300 | 9 | 8 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0007 | 0/0 | 6298 | 10 | 2 | 0 | 8 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0009 | 0/0 | 6297 | 8 | 8 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0010 | 0/0 | 6299 | 7 | 7 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0011 | 0/0 | 6292 | 4 | 4 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0013 | 0/0 | 6297 | 5 | 3 | 0 | 2 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0014 | 0/0 | 6297 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0015 | 0/0 | 6300 | 3 | 2 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0016 | 0/0 | 6299 | 3 | 0 | 0 | 3 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0017 | 0/0 | 6298 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0020 | 0/0 | 6295 | 2 | 2 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0023 | 1/0 | 6297 | 2 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0024 | 0/0 | 6297 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0027 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0030 | 0/0 | 6299 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0031 | 0/0 | 6299 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0032 | 0/0 | 6299 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0033 | 0/0 | 6299 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0035 | 0/0 | 6299 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0037 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0038 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0039 | 0/0 | 6298 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0042 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0001t0044 | 0/0 | 6297 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0002t0001 | 0/1 | 6297 | 66 | 3 | 11 | 35 | 5 | 11 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0002t0008 | 0/0 | 6296 | 8 | 0 | 0 | 6 | 0 | 2 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0002t0018 | 0/0 | 6298 | 3 | 0 | 0 | 3 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0002t0025 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0003t0002 | 0/0 | 6299 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0003t0004 | 0/0 | 6298 | 26 | 1 | 3 | 19 | 0 | 3 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0003t0014 | 0/0 | 6297 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0003t0019 | 0/0 | 6298 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0003t0041 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0008t0003 | 0/0 | 6299 | 3 | 0 | 1 | 0 | 2 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0010t0001 | 0/0 | 6297 | 2 | 0 | 1 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0011t0002 | 0/0 | 6299 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0014t0003 | 0/0 | 6299 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0018t0002 | 0/0 | 6299 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0001c0024t0002 | 0/0 | 6299 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0002c0004t0005 | 0/0 | 6301 | 14 | 0 | 9 | 1 | 1 | 3 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0002c0004t0012 | 0/0 | 6300 | 5 | 0 | 4 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0002c0004t0028 | 0/0 | 6301 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0003c0005t0022 | 0/0 | 6297 | 2 | 2 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0003c0005t0026 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0003c0005t0034 | 0/0 | 6299 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0003c0005t0040 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0003c0005t0043 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0004c0006t0004 | 0/0 | 6298 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0004c0006t0014 | 0/0 | 6297 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0005c0009t0011 | 0/0 | 6292 | 3 | 3 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0006c0007t0006 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0006c0007t0014 | 0/0 | 6297 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0006c0007t0029 | 0/0 | 6301 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0007c0012t0021 | 0/0 | 6299 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0008c0017t0001 | 0/0 | 5858 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0009c0019t0021 | 0/0 | 6299 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0010c0020t0036 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0011c0021t0003 | 0/0 | 6299 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0012c0022t0008 | 0/0 | 6296 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0013c0016t0003 | 0/0 | 6299 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0014c0023t0004 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0015c0015t0004 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0016c0025t0002 | 0/0 | 6299 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| a0017c0013t0002 | 0/0 | 6299 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | copy fasta | chr18 | 66496083 | 66609090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0010g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0011g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0011g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0013g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0013g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0014g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0015g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0015g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0015g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0016g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0016g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0017g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0017g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0017g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0020g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0023g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0023g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0024g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0027g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0030g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0031g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0032g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0033g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0035g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0037g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0038g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0039g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0042g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0001t0044g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0008g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0008g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0008g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0018g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0018g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0018g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0002t0025g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0014g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0019g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0019g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0019g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0003t0041g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0008t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0008t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0008t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0010t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0010t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0011t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0014t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0018t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0001c0024t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0005g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0012g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0012g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0012g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0012g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0012g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0002c0004t0028g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0003c0005t0022g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0003c0005t0022g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0003c0005t0026g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0003c0005t0034g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0003c0005t0040g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0003c0005t0043g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0004c0006t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0004c0006t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0004c0006t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0004c0006t0014g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0005c0009t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0005c0009t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0005c0009t0011g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0006c0007t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0006c0007t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0006c0007t0029g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0007c0012t0021g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0008c0017t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0009c0019t0021g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0010c0020t0036g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0011c0021t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0012c0022t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0013c0016t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0014c0023t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0015c0015t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0016c0025t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| a0017c0013t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0323 | EUR | GBR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00099 | hp2 | a0008 | c0017 | t0001 | g0331 | EUR | GBR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0345 | EUR | GBR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00140 | hp2 | a0007 | c0012 | t0021 | g0090 | EUR | GBR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0332 | EUR | FIN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00280 | hp2 | a0001 | c0008 | t0003 | g0302 | EUR | FIN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00323 | hp1 | a0001 | c0010 | t0001 | g0280 | EUR | FIN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00323 | hp2 | a0001 | c0008 | t0003 | g0303 | EUR | FIN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0351 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00438 | hp2 | a0001 | c0001 | t0013 | g0069 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00544 | hp2 | a0001 | c0003 | t0004 | g0292 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0343 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00558 | hp2 | a0001 | c0001 | t0013 | g0057 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00621 | hp1 | a0001 | c0003 | t0004 | g0181 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00639 | hp1 | a0001 | c0003 | t0004 | g0144 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00642 | hp1 | a0001 | c0010 | t0001 | g0308 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00642 | hp2 | a0002 | c0004 | t0028 | g0178 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00673 | hp1 | a0002 | c0004 | t0005 | g0285 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00673 | hp2 | a0001 | c0001 | t0016 | g0086 | EAS | CHS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0165 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00735 | hp1 | a0017 | c0013 | t0002 | g0189 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0313 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00741 | hp1 | a0001 | c0011 | t0002 | g0306 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01070 | hp1 | a0002 | c0004 | t0012 | g0245 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01109 | hp1 | a0004 | c0006 | t0014 | g0235 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01109 | hp2 | a0001 | c0001 | t0031 | g0294 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0286 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01167 | hp2 | a0002 | c0004 | t0012 | g0279 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01169 | hp2 | a0002 | c0004 | t0005 | g0278 | AMR | PUR | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01255 | hp2 | a0001 | c0001 | t0024 | g0003 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01257 | hp2 | a0001 | c0001 | t0014 | g0076 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01258 | hp1 | a0002 | c0004 | t0005 | g0284 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0075 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01261 | hp1 | a0012 | c0022 | t0008 | g0291 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01346 | hp2 | a0002 | c0004 | t0005 | g0276 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01358 | hp1 | a0001 | c0003 | t0004 | g0143 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01358 | hp2 | a0002 | c0004 | t0005 | g0252 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01361 | hp2 | a0002 | c0004 | t0005 | g0275 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01433 | hp1 | a0001 | c0001 | t0039 | g0319 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01433 | hp2 | a0001 | c0008 | t0003 | g0304 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01496 | hp1 | a0002 | c0004 | t0012 | g0282 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | CLM | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0311 | EUR | IBS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0084 | EUR | IBS | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01884 | hp1 | a0009 | c0019 | t0021 | g0310 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01891 | hp1 | a0004 | c0006 | t0004 | g0024 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0236 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01928 | hp1 | a0001 | c0001 | t0015 | g0048 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01943 | hp2 | a0002 | c0004 | t0005 | g0283 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01952 | hp1 | a0002 | c0004 | t0012 | g0238 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01975 | hp1 | a0013 | c0016 | t0003 | g0042 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01975 | hp2 | a0001 | c0018 | t0002 | g0167 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01978 | hp1 | a0002 | c0004 | t0005 | g0277 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01981 | hp2 | a0002 | c0004 | t0005 | g0128 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02080 | hp1 | a0001 | c0003 | t0004 | g0169 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02083 | hp1 | a0001 | c0001 | t0042 | g0059 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02145 | hp2 | a0001 | c0001 | t0013 | g0217 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02155 | hp1 | a0001 | c0001 | t0007 | g0092 | EAS | CDX | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02155 | hp2 | a0001 | c0003 | t0004 | g0349 | EAS | CDX | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02257 | hp1 | a0001 | c0001 | t0044 | g0115 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02258 | hp1 | a0003 | c0005 | t0022 | g0227 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0109 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02273 | hp2 | a0001 | c0003 | t0004 | g0145 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02280 | hp2 | a0001 | c0001 | t0027 | g0180 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02293 | hp1 | a0002 | c0004 | t0005 | g0149 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02451 | hp1 | a0001 | c0001 | t0023 | g0190 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0016 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02523 | hp2 | a0001 | c0003 | t0004 | g0297 | EAS | KHV | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02602 | hp1 | a0001 | c0003 | t0004 | g0296 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02602 | hp2 | a0001 | c0002 | t0008 | g0198 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0022 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0116 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0192 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0139 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02738 | hp2 | a0002 | c0004 | t0005 | g0017 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0118 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0237 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02886 | hp2 | a0001 | c0001 | t0017 | g0137 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02895 | hp1 | a0006 | c0007 | t0006 | g0188 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0100 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02896 | hp2 | a0001 | c0001 | t0017 | g0018 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02897 | hp1 | a0006 | c0007 | t0029 | g0187 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02922 | hp1 | a0001 | c0001 | t0020 | g0001 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02965 | hp1 | a0001 | c0001 | t0035 | g0172 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02965 | hp2 | a0010 | c0020 | t0036 | g0009 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0130 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02970 | hp2 | a0005 | c0009 | t0011 | g0248 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0099 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03041 | hp2 | a0015 | c0015 | t0004 | g0098 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03098 | hp1 | a0004 | c0006 | t0004 | g0125 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0246 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03130 | hp2 | a0003 | c0005 | t0040 | g0126 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0008 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03139 | hp2 | a0005 | c0009 | t0011 | g0247 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03195 | hp1 | a0006 | c0007 | t0014 | g0191 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03209 | hp1 | a0001 | c0002 | t0025 | g0004 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03209 | hp2 | a0003 | c0005 | t0043 | g0228 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03225 | hp1 | a0001 | c0003 | t0019 | g0027 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03225 | hp2 | a0004 | c0006 | t0004 | g0150 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0239 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03239 | hp2 | a0002 | c0004 | t0005 | g0119 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0251 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0225 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03492 | hp1 | a0001 | c0002 | t0008 | g0032 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0209 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0014 | AFR | ESN | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03540 | hp2 | a0003 | c0005 | t0022 | g0346 | AFR | GWD | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0347 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0117 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0242 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03669 | hp1 | a0002 | c0004 | t0005 | g0298 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0316 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0054 | SAS | STU | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0273 | SAS | STU | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0183 | SAS | PJL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0040 | SAS | BEB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03834 | hp2 | a0001 | c0003 | t0004 | g0264 | SAS | BEB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03927 | hp2 | a0002 | c0004 | t0012 | g0305 | SAS | BEB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | STU | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | STU | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG04228 | hp1 | a0001 | c0003 | t0004 | g0185 | SAS | STU | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0344 | SAS | STU | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0250 | AFR | YRI | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18522 | hp2 | a0001 | c0003 | t0019 | g0028 | AFR | YRI | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18747 | hp1 | a0001 | c0003 | t0014 | g0041 | EAS | CHB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | CHB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18906 | hp1 | a0001 | c0001 | t0017 | g0182 | AFR | YRI | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | YRI | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18939 | hp1 | a0001 | c0003 | t0004 | g0220 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18944 | hp1 | a0001 | c0003 | t0004 | g0037 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18945 | hp2 | a0001 | c0003 | t0004 | g0269 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18947 | hp1 | a0014 | c0023 | t0004 | g0216 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18949 | hp2 | a0001 | c0002 | t0018 | g0340 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18950 | hp1 | a0001 | c0002 | t0008 | g0194 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18952 | hp1 | a0001 | c0003 | t0004 | g0019 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18956 | hp1 | a0001 | c0001 | t0033 | g0341 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18957 | hp1 | a0001 | c0001 | t0030 | g0295 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18962 | hp1 | a0001 | c0003 | t0004 | g0132 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18962 | hp2 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18969 | hp2 | a0001 | c0002 | t0008 | g0196 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18971 | hp1 | a0001 | c0002 | t0008 | g0261 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18974 | hp1 | a0001 | c0001 | t0007 | g0268 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18979 | hp1 | a0001 | c0003 | t0004 | g0197 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18979 | hp2 | a0001 | c0024 | t0002 | g0134 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18985 | hp1 | a0001 | c0003 | t0004 | g0038 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18988 | hp2 | a0001 | c0001 | t0016 | g0327 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18990 | hp1 | a0001 | c0014 | t0003 | g0314 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18993 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18998 | hp1 | a0011 | c0021 | t0003 | g0272 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18998 | hp2 | a0001 | c0002 | t0008 | g0127 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18999 | hp1 | a0001 | c0003 | t0041 | g0170 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19006 | hp2 | a0001 | c0002 | t0018 | g0257 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19009 | hp1 | a0001 | c0003 | t0004 | g0039 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19009 | hp2 | a0001 | c0002 | t0008 | g0214 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | LWK | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19030 | hp2 | a0001 | c0001 | t0038 | g0124 | AFR | LWK | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19057 | hp1 | a0001 | c0001 | t0032 | g0200 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19062 | hp1 | a0001 | c0002 | t0008 | g0325 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19064 | hp2 | a0001 | c0001 | t0016 | g0342 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19066 | hp2 | a0001 | c0003 | t0004 | g0267 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0047 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19074 | hp1 | a0001 | c0002 | t0018 | g0036 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19079 | hp2 | a0001 | c0003 | t0004 | g0152 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19081 | hp2 | a0001 | c0003 | t0004 | g0184 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19086 | hp1 | a0001 | c0003 | t0004 | g0020 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19087 | hp1 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA19091 | hp2 | a0001 | c0003 | t0004 | g0218 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20129 | hp1 | a0001 | c0003 | t0019 | g0029 | AFR | ASW | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0244 | AFR | ASW | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0317 | EUR | TSI | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20752 | hp2 | a0002 | c0004 | t0005 | g0329 | EUR | TSI | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0240 | EUR | TSI | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0289 | EUR | TSI | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | GIH | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0161 | SAS | GIH | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02109 | hp1 | a0001 | c0001 | t0037 | g0212 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0219 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02559 | hp1 | a0005 | c0009 | t0011 | g0025 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG02559 | hp2 | a0003 | c0005 | t0026 | g0010 | AFR | ACB | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03471 | hp1 | a0001 | c0001 | t0020 | g0001 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG03471 | hp2 | a0016 | c0025 | t0002 | g0096 | AFR | MSL | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | USA | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | USA | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA18955 | hp2 | a0001 | c0003 | t0004 | g0171 | EAS | JPT | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20300 | hp1 | a0001 | c0003 | t0004 | g0151 | AFR | USA | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0322 | AFR | USA | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | LWK | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| NA21309 | hp2 | a0003 | c0005 | t0034 | g0113 | AFR | LWK | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0318 | REF | REF | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0023 | g0155 | REF | REF | CDH19_chr18_66496083_66609090 | CDH19 | chr18 | 66496083 | 66609090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:66504997
|
C | T | 1 | a0010 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2134G>A | p.Ala712Thr | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2383/6297 | 2134/2319 | 712/772 | chr18 | 66504997 | ||
| chr18:66505173
|
G | T | 1 | a0004 | 4 | HG01109.hp1 HG01891.hp1 HG03098.hp1 others(1): Show |
missense_variant | MODERATE | c.1958C>A | p.Ala653Asp | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2207/6297 | 1958/2319 | 653/772 | chr18 | 66505173 | ||
| chr18:66505197
|
C | G | 2 | a0007a0009 | 2 | HG00140.hp2 HG01884.hp1 |
missense_variant | MODERATE | c.1934G>C | p.Gly645Ala | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2183/6297 | 1934/2319 | 645/772 | chr18 | 66505197 | ||
| chr18:66511636
|
T | C | 1 | a0011 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.1508A>G | p.His503Arg | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/12 | 1757/6297 | 1508/2319 | 503/772 | chr18 | 66511636 | ||
| chr18:66543238
|
AGGATGGT others(4633): Show |
A | 1 | a0008 | 1 | HG00099.hp2 | exon_loss_variant | HIGH | c.776-2975_1214+732d others(2): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/12 | chr18 | 66543238 | ||||||
| chr18:66544014
|
C | T | 1 | a0002 | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
missense_variant | MODERATE | c.1171G>A | p.Val391Met | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/12 | 1420/6297 | 1171/2319 | 391/772 | chr18 | 66544014 | ||
| chr18:66544208
|
T | G | 1 | a0012 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.977A>C | p.His326Pro | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/12 | 1226/6297 | 977/2319 | 326/772 | chr18 | 66544208 | ||
| chr18:66554405
|
C | G | 1 | a0013 | 1 | HG01975.hp1 | missense_variant&splice_region_variant | MODERATE | c.610G>C | p.Gly204Arg | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/12 | 859/6297 | 610/2319 | 204/772 | chr18 | 66554405 | ||
| chr18:66568443
|
C | A | 1 | a0014 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.463G>T | p.Ala155Ser | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/12 | 712/6297 | 463/2319 | 155/772 | chr18 | 66568443 | ||
| chr18:66568455
|
C | G | 1 | a0015 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.451G>C | p.Glu151Gln | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/12 | 700/6297 | 451/2319 | 151/772 | chr18 | 66568455 | ||
| chr18:66568640
|
G | A | 1 | a0005 | 3 | HG02559.hp1 HG02970.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.266C>T | p.Thr89Ile | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/12 | 515/6297 | 266/2319 | 89/772 | chr18 | 66568640 | ||
| chr18:66568685
|
T | C | 1 | a0016 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.221A>G | p.Asn74Ser | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/12 | 470/6297 | 221/2319 | 74/772 | chr18 | 66568685 | ||
| chr18:66568693
|
G | T | 1 | a0017 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.213C>A | p.Asp71Glu | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/12 | 462/6297 | 213/2319 | 71/772 | chr18 | 66568693 | ||
| chr18:66572064
|
C | G | 1 | a0007 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.141G>C | p.Trp47Cys | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/12 | 390/6297 | 141/2319 | 47/772 | chr18 | 66572064 | ||
| chr18:66572132
|
T | C | 1 | a0003 | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
missense_variant | MODERATE | c.73A>G | p.Asn25Asp | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/12 | 322/6297 | 73/2319 | 25/772 | chr18 | 66572132 | ||
| chr18:66572150
|
A | T | 1 | a0006 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.55T>A | p.Cys19Ser | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/12 | 304/6297 | 55/2319 | 19/772 | chr18 | 66572150 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:66509032
|
G | A | 4 | a0001c0003a0001c0018a0004c0006others(1): Show | 38 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(35): Show |
synonymous_variant | LOW | c.1791C>T | p.Val597Val | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/12 | 2040/6297 | 1791/2319 | 597/772 | chr18 | 66509032 | ||
| chr18:66509128
|
G | T | 4 | a0001c0002a0001c0010a0008c0017others(1): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
synonymous_variant | LOW | c.1695C>A | p.Thr565Thr | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/12 | 1944/6297 | 1695/2319 | 565/772 | chr18 | 66509128 | ||
| chr18:66509149
|
C | T | 1 | a0001c0008 | 3 | HG00280.hp2 HG00323.hp2 HG01433.hp2 |
synonymous_variant | LOW | c.1674G>A | p.Pro558Pro | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/12 | 1923/6297 | 1674/2319 | 558/772 | chr18 | 66509149 | ||
| chr18:66529872
|
A | G | 1 | a0001c0018 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.1431T>C | p.Tyr477Tyr | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/12 | 1680/6297 | 1431/2319 | 477/772 | chr18 | 66529872 | ||
| chr18:66554451
|
G | A | 1 | a0003c0005 | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
synonymous_variant | LOW | c.564C>T | p.Tyr188Tyr | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/12 | 813/6297 | 564/2319 | 188/772 | chr18 | 66554451 | ||
| chr18:66554514
|
A | G | 1 | a0003c0005 | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
synonymous_variant | LOW | c.501T>C | p.Val167Val | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/12 | 750/6297 | 501/2319 | 167/772 | chr18 | 66554514 | ||
| chr18:66568468
|
T | C | 1 | a0001c0024 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.438A>G | p.Pro146Pro | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/12 | 687/6297 | 438/2319 | 146/772 | chr18 | 66568468 | ||
| chr18:66568507
|
C | T | 1 | a0001c0014 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.399G>A | p.Glu133Glu | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/12 | 648/6297 | 399/2319 | 133/772 | chr18 | 66568507 | ||
| chr18:66572172
|
C | T | 2 | a0001c0010a0001c0011 | 3 | HG00323.hp1 HG00642.hp1 HG00741.hp1 |
synonymous_variant | LOW | c.33G>A | p.Leu11Leu | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/12 | 282/6297 | 33/2319 | 11/772 | chr18 | 66572172 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:66501119
|
T | C | 1 | a0001c0001t0044 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3693A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 3693 | chr18 | 66501119 | |||||
| chr18:66501288
|
G | A | 1 | a0001c0003t0019 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3524C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 3524 | chr18 | 66501288 | |||||
| chr18:66501424
|
A | T | 1 | a0001c0001t0031 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3388T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 3388 | chr18 | 66501424 | |||||
| chr18:66501760
|
T | C | 1 | a0001c0001t0035 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3052A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 3052 | chr18 | 66501760 | |||||
| chr18:66501779
|
G | A | 7 | a0001c0002t0001a0001c0002t0008a0001c0002t0018others(4): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3033C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 3033 | chr18 | 66501779 | |||||
| chr18:66501823
|
A | C | 1 | a0010c0020t0036 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2989T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2989 | chr18 | 66501823 | |||||
| chr18:66501918
|
G | T | 1 | a0001c0001t0030 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2894 | chr18 | 66501918 | |||||
| chr18:66501933
|
T | A | 1 | a0001c0001t0016 | 3 | HG00673.hp2 NA18988.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2879A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2879 | chr18 | 66501933 | |||||
| chr18:66501962
|
T | C | 1 | a0001c0001t0039 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2850A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2850 | chr18 | 66501962 | |||||
| chr18:66502019
|
G | A | 1 | a0001c0001t0027 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2793C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2793 | chr18 | 66502019 | |||||
| chr18:66502107
|
T | C | 66 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*2705A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2705 | chr18 | 66502107 | |||||
| chr18:66502230
|
G | A | 1 | a0001c0003t0041 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2582C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2582 | chr18 | 66502230 | |||||
| chr18:66502349
|
A | C | 1 | a0001c0001t0037 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2463T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2463 | chr18 | 66502349 | |||||
| chr18:66502536
|
C | T | 1 | a0001c0001t0038 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2276G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 2276 | chr18 | 66502536 | |||||
| chr18:66502855
|
T | C | 1 | a0001c0001t0042 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1957A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1957 | chr18 | 66502855 | |||||
| chr18:66502925
|
G | A | 28 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(25): Show | 146 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1887C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1887 | chr18 | 66502925 | |||||
| chr18:66502947
|
G | A | 17 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(14): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1865C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1865 | chr18 | 66502947 | |||||
| chr18:66503155
|
C | T | 66 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1657G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1657 | chr18 | 66503155 | |||||
| chr18:66503214
|
C | G | 1 | a0001c0001t0037 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1598G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1598 | chr18 | 66503214 | |||||
| chr18:66503215
|
G | A | 2 | a0007c0012t0021a0009c0019t0021 | 2 | HG00140.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1597C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1597 | chr18 | 66503215 | |||||
| chr18:66503482
|
C | T | 1 | a0001c0001t0017 | 3 | HG02886.hp2 HG02896.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1330G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1330 | chr18 | 66503482 | |||||
| chr18:66503513
|
G | C | 1 | a0002c0004t0028 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1299C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1299 | chr18 | 66503513 | |||||
| chr18:66503580
|
A | C | 4 | a0002c0004t0005a0002c0004t0012a0002c0004t0028others(1): Show | 21 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1232T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1232 | chr18 | 66503580 | |||||
| chr18:66503627
|
G | A | 1 | a0001c0001t0032 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1185C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1185 | chr18 | 66503627 | |||||
| chr18:66503715
|
T | C | 1 | a0001c0001t0033 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1097A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1097 | chr18 | 66503715 | |||||
| chr18:66503746
|
T | G | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(33): Show | 161 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1066A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 1066 | chr18 | 66503746 | |||||
| chr18:66503847
|
G | C | 1 | a0003c0005t0043 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*965C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 965 | chr18 | 66503847 | |||||
| chr18:66504041
|
G | A | 2 | a0001c0001t0009a0001c0001t0044 | 9 | HG02257.hp1 HG02486.hp2 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*771C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 771 | chr18 | 66504041 | |||||
| chr18:66504274
|
G | T | 66 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*538C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 538 | chr18 | 66504274 | |||||
| chr18:66504291
|
C | CT | 19 | a0001c0001t0004a0001c0001t0007a0001c0001t0017others(16): Show | 77 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*520dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 520 | chr18 | 66504291 | |||||
| chr18:66504291
|
C | CTT | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(20): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*519_*520dupAA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 520 | chr18 | 66504291 | |||||
| chr18:66504291
|
C | CTTT | 4 | a0001c0001t0006a0001c0001t0015a0002c0004t0012others(1): Show | 18 | HG01070.hp1 HG01167.hp2 HG01496.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*518_*520dupAAA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 520 | chr18 | 66504291 | |||||
| chr18:66504291
|
C | CTTTT | 3 | a0002c0004t0005a0002c0004t0028a0006c0007t0029 | 16 | HG00642.hp2 HG00673.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*520dupAAAA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 520 | chr18 | 66504291 | |||||
| chr18:66504291
|
CT | C | 2 | a0001c0002t0008a0012c0022t0008 | 9 | HG01261.hp1 HG02602.hp2 HG03492.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*520delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 520 | chr18 | 66504291 | |||||
| chr18:66504291
|
CTTTTT | C | 2 | a0001c0001t0011a0005c0009t0011 | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*516_*520delAAAAA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 516 | chr18 | 66504291 | |||||
| chr18:66504346
|
A | G | 1 | a0001c0001t0027 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 466 | chr18 | 66504346 | |||||
| chr18:66504480
|
C | T | 3 | a0001c0001t0010a0001c0001t0024a0003c0005t0026 | 9 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 332 | chr18 | 66504480 | |||||
| chr18:66504603
|
G | C | 1 | a0001c0001t0020 | 2 | HG02922.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*209C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 12/12 | 209 | chr18 | 66504603 | |||||
| chr18:66604052
|
TCA | T | 3 | a0001c0001t0020a0001c0001t0024a0001c0002t0025 | 4 | HG01255.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-213_-212delTG | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/12 | 31849 | chr18 | 66604052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:66505389
|
T | C | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1829-87A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505389 | ||||||
| chr18:66505526
|
AATATAGT others(47): Show |
A | 1 | a0001c0002t0001g0293 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1829-278_1829-225d others(56): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505526 | ||||||
| chr18:66505543
|
TTATTAAT others(5): Show |
T | 1 | a0001c0003t0004g0020 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1829-253_1829-242d others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505543 | ||||||
| chr18:66505552
|
T | C | 1 | a0001c0003t0019g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1829-250A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505552 | ||||||
| chr18:66505560
|
A | AAT | 10 | a0001c0001t0002g0034a0001c0001t0002g0085a0001c0001t0002g0087others(7): Show | 10 | HG02132.hp1 HG03927.hp1 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.1829-260_1829-259d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505560 | ||||||
| chr18:66505560
|
AAT | A | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1829-260_1829-259d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505560 | ||||||
| chr18:66505585
|
A | T | 1 | a0001c0002t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1829-283T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505585 | ||||||
| chr18:66505635
|
TC | T | 82 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1829-334delG | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505635 | ||||||
| chr18:66505689
|
C | T | 43 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0003t0002g0008others(40): Show | 43 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1829-387G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505689 | ||||||
| chr18:66505770
|
A | G | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1829-468T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505770 | ||||||
| chr18:66505784
|
T | A | 2 | a0001c0002t0001g0323a0001c0002t0001g0332 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1829-482A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505784 | ||||||
| chr18:66505871
|
T | G | 2 | a0001c0003t0004g0169a0001c0003t0004g0197 | 2 | HG02080.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1829-569A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505871 | ||||||
| chr18:66505905
|
A | G | 1 | a0001c0001t0035g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1829-603T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505905 | ||||||
| chr18:66505927
|
A | G | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1829-625T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505927 | ||||||
| chr18:66505986
|
T | C | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1829-684A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66505986 | ||||||
| chr18:66506016
|
A | T | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1829-714T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506016 | ||||||
| chr18:66506017
|
G | A | 1 | a0001c0001t0009g0118 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1829-715C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506017 | ||||||
| chr18:66506204
|
A | G | 1 | a0001c0024t0002g0134 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1829-902T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506204 | ||||||
| chr18:66506260
|
G | A | 22 | a0001c0011t0002g0306a0002c0004t0005g0017a0002c0004t0005g0119others(19): Show | 22 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1829-958C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506260 | ||||||
| chr18:66506262
|
A | G | 2 | a0001c0002t0001g0140a0001c0002t0001g0141 | 2 | NA18950.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1829-960T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506262 | ||||||
| chr18:66506305
|
G | A | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1829-1003C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506305 | ||||||
| chr18:66506412
|
A | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1829-1110T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506412 | ||||||
| chr18:66506613
|
T | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1829-1311A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506613 | ||||||
| chr18:66506782
|
A | G | 1 | a0003c0005t0022g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1829-1480T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506782 | ||||||
| chr18:66506862
|
T | C | 1 | a0001c0001t0031g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1829-1560A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506862 | ||||||
| chr18:66506917
|
T | C | 3 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0017g0182 | 3 | HG02886.hp2 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1829-1615A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66506917 | ||||||
| chr18:66507029
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1829-1727G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66507029 | ||||||
| chr18:66507154
|
A | G | 2 | a0001c0001t0002g0337a0001c0011t0002g0306 | 2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1828+1841T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66507154 | ||||||
| chr18:66507261
|
G | C | 1 | a0001c0001t0002g0056 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1828+1734C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66507261 | ||||||
| chr18:66507285
|
T | TG | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1828+1709dupC | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66507285 | ||||||
| chr18:66507468
|
C | G | 1 | a0001c0002t0001g0307 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1828+1527G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66507468 | ||||||
| chr18:66507587
|
G | A | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828+1408C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66507587 | ||||||
| chr18:66507624
|
G | A | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1828+1371C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66507624 | ||||||
| chr18:66507991
|
A | C | 9 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(6): Show | 9 | HG02257.hp1 HG02486.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1828+1004T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66507991 | ||||||
| chr18:66508030
|
G | A | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1828+965C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508030 | ||||||
| chr18:66508089
|
T | A | 1 | a0001c0001t0020g0001 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1828+906A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508089 | ||||||
| chr18:66508325
|
C | T | 74 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(71): Show | 74 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1828+670G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508325 | ||||||
| chr18:66508341
|
G | C | 1 | a0001c0001t0006g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1828+654C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508341 | ||||||
| chr18:66508342
|
T | A | 128 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(125): Show | 128 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1828+653A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508342 | ||||||
| chr18:66508395
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1828+600G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508395 | ||||||
| chr18:66508399
|
G | GT | 121 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(118): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1828+595dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508399 | ||||||
| chr18:66508430
|
G | A | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1828+565C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508430 | ||||||
| chr18:66508462
|
G | A | 6 | a0001c0001t0035g0172a0003c0005t0022g0227a0003c0005t0022g0346others(3): Show | 6 | HG02258.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1828+533C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508462 | ||||||
| chr18:66508551
|
G | A | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1828+444C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508551 | ||||||
| chr18:66508677
|
A | T | 3 | a0001c0003t0004g0039a0001c0003t0004g0267a0001c0003t0004g0269 | 3 | NA18945.hp2 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1828+318T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508677 | ||||||
| chr18:66508753
|
T | TACACACT others(1): Show |
347 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(344): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1828+241_1828+242i others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508753 | ||||||
| chr18:66508770
|
C | T | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1828+225G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508770 | ||||||
| chr18:66508788
|
C | T | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1828+207G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508788 | ||||||
| chr18:66508810
|
T | G | 142 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(139): Show | 143 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1828+185A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508810 | ||||||
| chr18:66508974
|
G | A | 3 | a0001c0003t0004g0152a0001c0003t0004g0185a0001c0003t0014g0041 | 3 | HG04228.hp1 NA18747.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1828+21C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 11/11 | chr18 | 66508974 | ||||||
| chr18:66509306
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1577-60A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66509306 | ||||||
| chr18:66509350
|
A | G | 1 | a0001c0001t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1577-104T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66509350 | ||||||
| chr18:66509382
|
C | T | 143 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(140): Show | 144 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1577-136G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66509382 | ||||||
| chr18:66509429
|
T | C | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1577-183A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66509429 | ||||||
| chr18:66509444
|
T | A | 1 | a0001c0001t0002g0312 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1577-198A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66509444 | ||||||
| chr18:66509454
|
A | G | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1577-208T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66509454 | ||||||
| chr18:66509524
|
TTTAG | T | 3 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0017g0182 | 3 | HG02886.hp2 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1577-282_1577-279d others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66509524 | ||||||
| chr18:66509677
|
T | A | 337 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1577-431A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66509677 | ||||||
| chr18:66510006
|
A | G | 8 | a0001c0001t0002g0026a0001c0001t0006g0013a0001c0001t0006g0073others(5): Show | 8 | HG01884.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1577-760T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510006 | ||||||
| chr18:66510012
|
T | A | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1577-766A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510012 | ||||||
| chr18:66510222
|
G | C | 1 | a0001c0002t0001g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1577-976C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510222 | ||||||
| chr18:66510322
|
C | T | 82 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1577-1076G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510322 | ||||||
| chr18:66510583
|
A | AAAT | 17 | a0001c0001t0002g0051a0001c0001t0002g0056a0001c0001t0002g0068others(14): Show | 17 | HG00280.hp1 HG01261.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1576+982_1576+984d others(5): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510583 | ||||||
| chr18:66510583
|
AAAT | A | 119 | a0001c0001t0002g0034a0001c0001t0002g0078a0001c0001t0002g0085others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1576+982_1576+984d others(5): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510583 | ||||||
| chr18:66510583
|
AAATAAT | A | 75 | a0001c0001t0002g0026a0001c0001t0002g0079a0001c0001t0002g0083others(72): Show | 76 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1576+979_1576+984d others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510583 | ||||||
| chr18:66510583
|
AAATAATA others(2): Show |
A | 75 | a0001c0001t0003g0002a0001c0001t0003g0011a0001c0001t0003g0035others(72): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1576+976_1576+984d others(11): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510583 | ||||||
| chr18:66510583
|
AAATAATA others(5): Show |
A | 2 | a0001c0001t0015g0246a0001c0001t0017g0137 | 2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1576+973_1576+984d others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510583 | ||||||
| chr18:66510583
|
AAATAATA others(11): Show |
A | 1 | a0001c0001t0003g0249 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1576+967_1576+984d others(20): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510583 | ||||||
| chr18:66510583
|
AAATAATA others(14): Show |
A | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1576+964_1576+984d others(23): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510583 | ||||||
| chr18:66510664
|
G | T | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1576+904C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510664 | ||||||
| chr18:66510819
|
C | T | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1576+749G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510819 | ||||||
| chr18:66510911
|
C | G | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1576+657G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66510911 | ||||||
| chr18:66511193
|
T | C | 350 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(347): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1576+375A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511193 | ||||||
| chr18:66511198
|
C | CTG | 337 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1576+369_1576+370i others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511198 | ||||||
| chr18:66511293
|
A | G | 38 | a0001c0003t0002g0008a0001c0003t0004g0019a0001c0003t0004g0020others(35): Show | 38 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1576+275T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511293 | ||||||
| chr18:66511298
|
C | T | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1576+270G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511298 | ||||||
| chr18:66511331
|
GC | G | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1576+236delG | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511331 | ||||||
| chr18:66511334
|
A | T | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1576+234T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511334 | ||||||
| chr18:66511337
|
G | A | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1576+231C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511337 | ||||||
| chr18:66511339
|
T | A | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1576+229A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511339 | ||||||
| chr18:66511340
|
A | C | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1576+228T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 10/11 | chr18 | 66511340 | ||||||
| chr18:66511832
|
T | C | 10 | a0001c0001t0002g0034a0001c0001t0002g0085a0001c0001t0002g0087others(7): Show | 10 | HG02132.hp1 HG03927.hp1 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.1459-147A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66511832 | ||||||
| chr18:66511839
|
G | GT | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1459-155dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66511839 | ||||||
| chr18:66512036
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1459-351T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512036 | ||||||
| chr18:66512201
|
A | C | 1 | a0001c0001t0027g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1459-516T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512201 | ||||||
| chr18:66512311
|
T | C | 337 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1459-626A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512311 | ||||||
| chr18:66512455
|
C | T | 337 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1459-770G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512455 | ||||||
| chr18:66512637
|
T | A | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1459-952A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512637 | ||||||
| chr18:66512673
|
GTTAA | G | 35 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(32): Show | 36 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1459-992_1459-989d others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512673 | ||||||
| chr18:66512813
|
T | G | 83 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(80): Show | 83 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1459-1128A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512813 | ||||||
| chr18:66512828
|
T | A | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1459-1143A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512828 | ||||||
| chr18:66512939
|
T | C | 8 | a0001c0001t0002g0026a0001c0001t0006g0013a0001c0001t0006g0073others(5): Show | 8 | HG01884.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459-1254A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66512939 | ||||||
| chr18:66513618
|
G | T | 38 | a0001c0003t0002g0008a0001c0003t0004g0019a0001c0003t0004g0020others(35): Show | 38 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1459-1933C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513618 | ||||||
| chr18:66513655
|
A | C | 82 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-1970T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513655 | ||||||
| chr18:66513674
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1459-1989C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513674 | ||||||
| chr18:66513713
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1459-2028C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513713 | ||||||
| chr18:66513753
|
A | C | 1 | a0001c0001t0003g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1459-2068T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513753 | ||||||
| chr18:66513792
|
A | G | 3 | a0001c0001t0007g0080a0001c0001t0007g0081a0001c0001t0007g0092 | 3 | HG02155.hp1 NA18969.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1459-2107T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513792 | ||||||
| chr18:66513825
|
A | C | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1459-2140T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513825 | ||||||
| chr18:66513874
|
C | T | 7 | a0001c0002t0001g0259a0001c0002t0001g0260a0001c0002t0001g0262others(4): Show | 7 | NA18949.hp2 NA18971.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459-2189G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513874 | ||||||
| chr18:66513878
|
G | A | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1459-2193C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513878 | ||||||
| chr18:66513941
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1459-2256T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66513941 | ||||||
| chr18:66514036
|
A | G | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1459-2351T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514036 | ||||||
| chr18:66514040
|
T | A | 2 | a0001c0001t0003g0249a0001c0001t0015g0246 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1459-2355A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514040 | ||||||
| chr18:66514262
|
A | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1459-2577T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514262 | ||||||
| chr18:66514284
|
C | A | 1 | a0003c0005t0022g0346 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1459-2599G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514284 | ||||||
| chr18:66514427
|
G | A | 3 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0017g0182 | 3 | HG02886.hp2 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1459-2742C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514427 | ||||||
| chr18:66514451
|
G | A | 1 | a0002c0004t0005g0252 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1459-2766C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514451 | ||||||
| chr18:66514512
|
C | T | 337 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1459-2827G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514512 | ||||||
| chr18:66514522
|
A | C | 1 | a0001c0001t0002g0034 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1459-2837T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514522 | ||||||
| chr18:66514676
|
A | G | 8 | a0001c0001t0002g0026a0001c0001t0006g0013a0001c0001t0006g0073others(5): Show | 8 | HG01884.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459-2991T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514676 | ||||||
| chr18:66514773
|
A | G | 35 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(32): Show | 36 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1459-3088T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514773 | ||||||
| chr18:66514812
|
C | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1459-3127G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514812 | ||||||
| chr18:66514863
|
T | A | 1 | a0001c0001t0002g0093 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1459-3178A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514863 | ||||||
| chr18:66514889
|
A | T | 1 | a0003c0005t0026g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1459-3204T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514889 | ||||||
| chr18:66514926
|
T | G | 1 | a0001c0002t0001g0174 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1459-3241A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514926 | ||||||
| chr18:66514948
|
T | G | 2 | a0001c0001t0003g0336a0001c0001t0013g0069 | 2 | HG00438.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1459-3263A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66514948 | ||||||
| chr18:66515045
|
G | T | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1459-3360C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66515045 | ||||||
| chr18:66515075
|
C | G | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1459-3390G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66515075 | ||||||
| chr18:66515103
|
A | C | 127 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(124): Show | 127 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1459-3418T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66515103 | ||||||
| chr18:66515146
|
A | T | 2 | a0001c0002t0001g0094a0008c0017t0001g0331 | 2 | HG00099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1459-3461T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66515146 | ||||||
| chr18:66515224
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1459-3539C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66515224 | ||||||
| chr18:66515348
|
T | C | 82 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-3663A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66515348 | ||||||
| chr18:66515598
|
C | A | 1 | a0001c0001t0011g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1459-3913G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66515598 | ||||||
| chr18:66515923
|
T | C | 8 | a0001c0001t0002g0026a0001c0001t0006g0013a0001c0001t0006g0073others(5): Show | 8 | HG01884.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459-4238A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66515923 | ||||||
| chr18:66516072
|
C | T | 6 | a0001c0001t0035g0172a0003c0005t0022g0227a0003c0005t0022g0346others(3): Show | 6 | HG02258.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1459-4387G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516072 | ||||||
| chr18:66516289
|
A | T | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1459-4604T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516289 | ||||||
| chr18:66516368
|
T | C | 3 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0017g0182 | 3 | HG02886.hp2 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1459-4683A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516368 | ||||||
| chr18:66516488
|
T | A | 3 | a0001c0001t0002g0301a0001c0001t0002g0333a0001c0001t0002g0334 | 3 | HG00438.hp1 NA18944.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1459-4803A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516488 | ||||||
| chr18:66516529
|
G | A | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1459-4844C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516529 | ||||||
| chr18:66516580
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1459-4895A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516580 | ||||||
| chr18:66516644
|
G | T | 1 | a0002c0004t0012g0305 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1459-4959C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516644 | ||||||
| chr18:66516665
|
T | G | 1 | a0001c0003t0004g0039 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1459-4980A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516665 | ||||||
| chr18:66516826
|
G | A | 1 | a0012c0022t0008g0291 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1459-5141C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516826 | ||||||
| chr18:66516827
|
T | C | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1459-5142A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66516827 | ||||||
| chr18:66517016
|
C | A | 8 | a0001c0001t0020g0001a0001c0001t0035g0172a0003c0005t0022g0227others(5): Show | 9 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1459-5331G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517016 | ||||||
| chr18:66517076
|
T | C | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1459-5391A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517076 | ||||||
| chr18:66517207
|
C | T | 2 | a0001c0010t0001g0280a0001c0010t0001g0308 | 2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.1459-5522G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517207 | ||||||
| chr18:66517247
|
C | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1459-5562G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517247 | ||||||
| chr18:66517372
|
T | C | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1459-5687A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517372 | ||||||
| chr18:66517713
|
G | A | 127 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(124): Show | 127 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1459-6028C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517713 | ||||||
| chr18:66517733
|
G | T | 1 | a0003c0005t0026g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1459-6048C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517733 | ||||||
| chr18:66517737
|
C | A | 82 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-6052G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517737 | ||||||
| chr18:66517739
|
T | C | 1 | a0001c0003t0004g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1459-6054A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517739 | ||||||
| chr18:66517827
|
T | A | 83 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(80): Show | 83 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1459-6142A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517827 | ||||||
| chr18:66517847
|
TA | T | 82 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-6163delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517847 | ||||||
| chr18:66517863
|
T | C | 1 | a0001c0001t0039g0319 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1459-6178A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517863 | ||||||
| chr18:66517931
|
C | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1459-6246G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66517931 | ||||||
| chr18:66518027
|
C | T | 1 | a0001c0014t0003g0314 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1459-6342G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518027 | ||||||
| chr18:66518060
|
T | A | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1459-6375A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518060 | ||||||
| chr18:66518141
|
A | C | 6 | a0002c0004t0005g0275a0002c0004t0005g0276a0002c0004t0005g0277others(3): Show | 6 | HG01070.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1459-6456T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518141 | ||||||
| chr18:66518160
|
C | T | 1 | a0001c0001t0015g0237 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1459-6475G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518160 | ||||||
| chr18:66518286
|
T | C | 1 | a0001c0001t0003g0072 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1459-6601A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518286 | ||||||
| chr18:66518381
|
C | T | 83 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(80): Show | 83 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1459-6696G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518381 | ||||||
| chr18:66518388
|
C | T | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459-6703G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518388 | ||||||
| chr18:66518404
|
T | C | 1 | a0001c0001t0017g0137 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1459-6719A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518404 | ||||||
| chr18:66518446
|
C | T | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1459-6761G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518446 | ||||||
| chr18:66518513
|
C | T | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1459-6828G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518513 | ||||||
| chr18:66518749
|
G | A | 82 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-7064C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518749 | ||||||
| chr18:66518868
|
CTT | C | 91 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(88): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1459-7185_1459-718 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518868 | ||||||
| chr18:66518942
|
C | G | 8 | a0001c0001t0020g0001a0001c0001t0035g0172a0003c0005t0022g0227others(5): Show | 9 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1459-7257G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518942 | ||||||
| chr18:66518979
|
A | C | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1459-7294T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518979 | ||||||
| chr18:66518981
|
G | A | 5 | a0001c0001t0002g0203a0001c0001t0002g0208a0001c0001t0002g0211others(2): Show | 5 | HG02083.hp2 HG03492.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1459-7296C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66518981 | ||||||
| chr18:66519047
|
C | T | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1459-7362G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519047 | ||||||
| chr18:66519065
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1459-7380G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519065 | ||||||
| chr18:66519171
|
T | C | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459-7486A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519171 | ||||||
| chr18:66519173
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1459-7488C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519173 | ||||||
| chr18:66519201
|
C | T | 1 | a0001c0002t0001g0043 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1459-7516G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519201 | ||||||
| chr18:66519266
|
C | T | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1459-7581G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519266 | ||||||
| chr18:66519428
|
C | CAGCATGG others(7): Show |
1 | a0001c0001t0003g0232 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1459-7757_1459-774 others(18): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519428 | ||||||
| chr18:66519482
|
A | T | 2 | a0001c0001t0002g0333a0001c0001t0002g0334 | 2 | NA18944.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1459-7797T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519482 | ||||||
| chr18:66519495
|
G | T | 8 | a0001c0001t0020g0001a0001c0001t0035g0172a0003c0005t0022g0227others(5): Show | 9 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1459-7810C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519495 | ||||||
| chr18:66519551
|
A | C | 1 | a0001c0001t0027g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1459-7866T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519551 | ||||||
| chr18:66519767
|
T | C | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1459-8082A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519767 | ||||||
| chr18:66519935
|
C | A | 38 | a0001c0003t0002g0008a0001c0003t0004g0019a0001c0003t0004g0020others(35): Show | 38 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1459-8250G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519935 | ||||||
| chr18:66519983
|
A | C | 1 | a0001c0001t0002g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1459-8298T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66519983 | ||||||
| chr18:66520168
|
C | T | 5 | a0001c0002t0001g0195a0001c0002t0008g0127a0001c0002t0008g0194others(2): Show | 5 | NA18950.hp1 NA18969.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1459-8483G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520168 | ||||||
| chr18:66520339
|
C | CT | 7 | a0001c0002t0001g0023a0001c0002t0001g0065a0001c0002t0001g0066others(4): Show | 7 | HG01981.hp1 NA18942.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459-8655dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520339 | ||||||
| chr18:66520340
|
TG | T | 5 | a0001c0002t0001g0033a0001c0002t0001g0140a0001c0002t0001g0244others(2): Show | 5 | HG01167.hp1 HG03491.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1459-8656delC | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520340 | ||||||
| chr18:66520341
|
G | GT | 40 | a0001c0001t0002g0089a0001c0001t0002g0101a0001c0001t0002g0133others(37): Show | 40 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1459-8657dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520341 | ||||||
| chr18:66520341
|
G | GTT | 94 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(91): Show | 95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1459-8658_1459-865 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520341 | ||||||
| chr18:66520341
|
G | GTTT | 9 | a0001c0001t0003g0123a0001c0001t0003g0230a0001c0001t0003g0350others(6): Show | 9 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1459-8659_1459-865 others(7): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520341 | ||||||
| chr18:66520341
|
G | T | 77 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0043others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1459-8656C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520341 | ||||||
| chr18:66520341
|
GT | G | 32 | a0001c0001t0002g0026a0001c0001t0006g0013a0001c0001t0006g0073others(29): Show | 33 | HG00673.hp1 HG01070.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1459-8657delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520341 | ||||||
| chr18:66520341
|
GTT | G | 11 | a0001c0001t0002g0274a0001c0001t0006g0105a0001c0001t0011g0014others(8): Show | 11 | HG01169.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1459-8658_1459-865 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520341 | ||||||
| chr18:66520358
|
T | C | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1459-8673A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520358 | ||||||
| chr18:66520374
|
G | A | 8 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(5): Show | 8 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459-8689C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520374 | ||||||
| chr18:66520426
|
G | C | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1459-8741C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520426 | ||||||
| chr18:66520468
|
GT | G | 91 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(88): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1459-8784delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520468 | ||||||
| chr18:66520621
|
T | C | 337 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1459-8936A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520621 | ||||||
| chr18:66520639
|
A | C | 8 | a0001c0001t0020g0001a0001c0001t0035g0172a0003c0005t0022g0227others(5): Show | 9 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1459-8954T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520639 | ||||||
| chr18:66520838
|
C | G | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1458+9007G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520838 | ||||||
| chr18:66520871
|
T | C | 8 | a0001c0001t0020g0001a0001c0001t0035g0172a0003c0005t0022g0227others(5): Show | 9 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1458+8974A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520871 | ||||||
| chr18:66520930
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1458+8915C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66520930 | ||||||
| chr18:66521042
|
T | C | 162 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(159): Show | 163 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1458+8803A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521042 | ||||||
| chr18:66521083
|
TC | T | 80 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1458+8761delG | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521083 | ||||||
| chr18:66521124
|
G | A | 350 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(347): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1458+8721C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521124 | ||||||
| chr18:66521140
|
C | G | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1458+8705G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521140 | ||||||
| chr18:66521211
|
C | A | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1458+8634G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521211 | ||||||
| chr18:66521334
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1458+8511A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521334 | ||||||
| chr18:66521441
|
T | C | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1458+8404A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521441 | ||||||
| chr18:66521471
|
G | T | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1458+8374C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521471 | ||||||
| chr18:66521502
|
C | CTTTA | 6 | a0001c0001t0003g0271a0001c0001t0003g0313a0001c0001t0031g0294others(3): Show | 6 | HG00735.hp2 HG01109.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1458+8339_1458+834 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521502 | ||||||
| chr18:66521502
|
C | CTTTATTT others(1): Show |
8 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(5): Show | 8 | HG00735.hp1 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1458+8335_1458+834 others(12): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521502 | ||||||
| chr18:66521523
|
T | TTTA | 34 | a0001c0001t0002g0093a0001c0001t0002g0352a0001c0001t0010g0012others(31): Show | 34 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1458+8321_1458+832 others(7): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521523 | ||||||
| chr18:66521523
|
T | TTTATTTA | 78 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1458+8321_1458+832 others(11): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521523 | ||||||
| chr18:66521523
|
T | TTTATTTA others(4): Show |
28 | a0001c0001t0002g0088a0001c0001t0002g0102a0001c0001t0002g0106others(25): Show | 28 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1458+8321_1458+832 others(15): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521523 | ||||||
| chr18:66521523
|
TTTTG | T | 98 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0003g0324others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1458+8318_1458+832 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521523 | ||||||
| chr18:66521526
|
T | A | 112 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(109): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1458+8319A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521526 | ||||||
| chr18:66521527
|
G | A | 140 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(137): Show | 140 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1458+8318C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521527 | ||||||
| chr18:66521527
|
G | C | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1458+8318C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521527 | ||||||
| chr18:66521527
|
G | T | 109 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1458+8318C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521527 | ||||||
| chr18:66521530
|
T | A | 6 | a0001c0001t0002g0089a0001c0001t0002g0135a0001c0001t0002g0136others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1458+8315A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521530 | ||||||
| chr18:66521530
|
T | TA | 138 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(135): Show | 138 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1458+8314_1458+831 others(5): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521530 | ||||||
| chr18:66521531
|
G | A | 2 | a0001c0001t0004g0344a0001c0001t0027g0180 | 2 | HG02280.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1458+8314C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521531 | ||||||
| chr18:66521531
|
G | T | 144 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(141): Show | 144 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1458+8314C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521531 | ||||||
| chr18:66521535
|
G | T | 2 | a0001c0001t0004g0344a0001c0001t0027g0180 | 2 | HG02280.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1458+8310C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521535 | ||||||
| chr18:66521702
|
A | C | 1 | a0001c0002t0001g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1458+8143T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521702 | ||||||
| chr18:66521704
|
T | TA | 10 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+8140dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521704 | ||||||
| chr18:66521736
|
A | T | 35 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(32): Show | 36 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1458+8109T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521736 | ||||||
| chr18:66521804
|
C | T | 1 | a0001c0001t0002g0055 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1458+8041G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521804 | ||||||
| chr18:66521805
|
T | C | 1 | a0001c0001t0002g0055 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1458+8040A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521805 | ||||||
| chr18:66521808
|
C | A | 1 | a0001c0001t0002g0055 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1458+8037G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521808 | ||||||
| chr18:66521916
|
C | CTGT | 9 | a0001c0001t0009g0117a0001c0001t0009g0130a0001c0001t0009g0219others(6): Show | 10 | HG02257.hp1 HG02486.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1458+7926_1458+792 others(7): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521916 | ||||||
| chr18:66521916
|
C | CTGTTGT | 4 | a0001c0001t0009g0116a0001c0001t0009g0146a0001c0001t0009g0192others(1): Show | 4 | HG02647.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1458+7923_1458+792 others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521916 | ||||||
| chr18:66521916
|
C | CTGTTTT | 46 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0002t0001g0023others(43): Show | 46 | HG00558.hp1 HG00741.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1458+7928_1458+792 others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521916 | ||||||
| chr18:66521916
|
C | CTGTTTTT others(2): Show |
6 | a0001c0002t0001g0063a0001c0002t0001g0120a0001c0002t0001g0122others(3): Show | 6 | HG00639.hp1 HG00738.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1458+7928_1458+792 others(13): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521916 | ||||||
| chr18:66521916
|
CTGT | C | 45 | a0001c0001t0002g0079a0001c0001t0002g0226a0001c0001t0002g0335others(42): Show | 45 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.1458+7926_1458+792 others(7): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521916 | ||||||
| chr18:66521916
|
CTGTTGT | C | 73 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(70): Show | 73 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1458+7923_1458+792 others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521916 | ||||||
| chr18:66521916
|
CTGTTGTT others(2): Show |
C | 74 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1458+7920_1458+792 others(13): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521916 | ||||||
| chr18:66521916
|
CTGTTGTT others(5): Show |
C | 15 | a0001c0001t0002g0034a0001c0001t0002g0085a0001c0001t0002g0087others(12): Show | 15 | HG00438.hp2 HG02132.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1458+7917_1458+792 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521916 | ||||||
| chr18:66521918
|
G | GTTT | 55 | a0001c0002t0001g0094a0001c0002t0001g0174a0001c0002t0001g0176others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1458+7926_1458+792 others(7): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521918 | ||||||
| chr18:66521921
|
G | T | 18 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0027g0180others(15): Show | 18 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1458+7924C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521921 | ||||||
| chr18:66521924
|
G | T | 6 | a0001c0001t0002g0079a0001c0001t0002g0226a0001c0001t0002g0335others(3): Show | 6 | HG01346.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1458+7921C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521924 | ||||||
| chr18:66521927
|
G | T | 68 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(65): Show | 68 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1458+7918C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521927 | ||||||
| chr18:66521933
|
G | T | 13 | a0001c0001t0002g0034a0001c0001t0002g0085a0001c0001t0002g0087others(10): Show | 13 | HG02132.hp1 HG03927.hp1 NA18964.hp2 others(10): Show |
intron_variant | MODIFIER | c.1458+7912C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521933 | ||||||
| chr18:66521936
|
G | A | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1458+7909C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521936 | ||||||
| chr18:66521985
|
C | T | 117 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1458+7860G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66521985 | ||||||
| chr18:66522089
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1458+7756C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522089 | ||||||
| chr18:66522096
|
G | A | 1 | a0001c0001t0038g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1458+7749C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522096 | ||||||
| chr18:66522126
|
T | G | 8 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(5): Show | 8 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1458+7719A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522126 | ||||||
| chr18:66522170
|
A | G | 84 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(81): Show | 84 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1458+7675T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522170 | ||||||
| chr18:66522262
|
G | C | 1 | a0003c0005t0026g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1458+7583C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522262 | ||||||
| chr18:66522318
|
C | T | 1 | a0002c0004t0012g0282 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1458+7527G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522318 | ||||||
| chr18:66522442
|
G | A | 92 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1458+7403C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522442 | ||||||
| chr18:66522443
|
G | T | 168 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(165): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1458+7402C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522443 | ||||||
| chr18:66522446
|
C | T | 38 | a0001c0003t0002g0008a0001c0003t0004g0019a0001c0003t0004g0020others(35): Show | 38 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1458+7399G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522446 | ||||||
| chr18:66522447
|
G | A | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1458+7398C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522447 | ||||||
| chr18:66522477
|
T | C | 2 | a0001c0002t0001g0244a0001c0002t0001g0286 | 2 | HG01167.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1458+7368A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522477 | ||||||
| chr18:66522516
|
T | C | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1458+7329A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522516 | ||||||
| chr18:66522640
|
T | C | 1 | a0003c0005t0040g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1458+7205A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522640 | ||||||
| chr18:66522641
|
A | G | 1 | a0003c0005t0022g0346 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1458+7204T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522641 | ||||||
| chr18:66522664
|
T | A | 82 | a0001c0002t0001g0023a0001c0002t0001g0030a0001c0002t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1458+7181A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522664 | ||||||
| chr18:66522857
|
T | C | 1 | a0001c0003t0004g0292 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1458+6988A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522857 | ||||||
| chr18:66522888
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1458+6957A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522888 | ||||||
| chr18:66522925
|
A | C | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1458+6920T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66522925 | ||||||
| chr18:66523273
|
T | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1458+6572A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523273 | ||||||
| chr18:66523610
|
G | A | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1458+6235C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523610 | ||||||
| chr18:66523615
|
G | T | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1458+6230C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523615 | ||||||
| chr18:66523618
|
G | A | 1 | a0001c0001t0007g0080 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1458+6227C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523618 | ||||||
| chr18:66523618
|
G | T | 3 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0274 | 3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1458+6227C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523618 | ||||||
| chr18:66523640
|
C | G | 10 | a0001c0001t0002g0034a0001c0001t0002g0085a0001c0001t0002g0087others(7): Show | 10 | HG02132.hp1 HG03927.hp1 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+6205G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523640 | ||||||
| chr18:66523716
|
G | C | 98 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0034others(95): Show | 99 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1458+6129C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523716 | ||||||
| chr18:66523758
|
G | GC | 3 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0035g0172 | 3 | HG02896.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1458+6086dupG | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523758 | ||||||
| chr18:66523810
|
T | G | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1458+6035A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523810 | ||||||
| chr18:66523815
|
A | C | 1 | a0004c0006t0004g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1458+6030T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523815 | ||||||
| chr18:66523922
|
TG | T | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1458+5922delC | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66523922 | ||||||
| chr18:66524036
|
T | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+5809A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524036 | ||||||
| chr18:66524536
|
T | TTG | 3 | a0002c0004t0005g0252a0002c0004t0005g0283a0002c0004t0005g0284 | 3 | HG01258.hp1 HG01358.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1458+5307_1458+530 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524536 | ||||||
| chr18:66524542
|
G | GTA | 13 | a0001c0001t0002g0026a0001c0001t0003g0035a0001c0001t0003g0070others(10): Show | 13 | HG01109.hp2 HG01255.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1458+5301_1458+530 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTATA | 13 | a0001c0001t0002g0079a0001c0001t0003g0313a0001c0001t0004g0095others(10): Show | 13 | HG00140.hp2 HG00673.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1458+5299_1458+530 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTATATA | 10 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(7): Show | 10 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1458+5297_1458+530 others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTATATAT others(1): Show |
10 | a0001c0001t0006g0112a0001c0001t0009g0130a0001c0001t0009g0146others(7): Show | 10 | HG00639.hp1 HG01358.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1458+5295_1458+530 others(12): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTATATAT others(3): Show |
4 | a0001c0018t0002g0167a0003c0005t0022g0227a0004c0006t0004g0024others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1458+5293_1458+530 others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTATATAT others(5): Show |
1 | a0003c0005t0022g0346 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1458+5291_1458+530 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTATATAT others(7): Show |
4 | a0001c0002t0001g0323a0001c0003t0004g0151a0004c0006t0004g0125others(1): Show | 4 | HG00099.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1458+5289_1458+530 others(18): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTATATAT others(9): Show |
1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1458+5287_1458+530 others(20): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTATATAT others(11): Show |
1 | a0001c0002t0001g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1458+5285_1458+530 others(22): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTGTATAT others(5): Show |
6 | a0001c0002t0001g0259a0001c0002t0001g0260a0001c0002t0001g0262others(3): Show | 6 | NA18949.hp2 NA18971.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.1458+5302_1458+530 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTGTATAT others(7): Show |
2 | a0001c0002t0001g0174a0001c0002t0001g0330 | 2 | NA18970.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1458+5302_1458+530 others(18): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTGTATAT others(9): Show |
2 | a0001c0002t0001g0222a0001c0002t0001g0343 | 2 | HG00558.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1458+5302_1458+530 others(20): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTGTATAT others(11): Show |
1 | a0001c0002t0001g0263 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1458+5302_1458+530 others(22): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
G | GTGTATAT others(13): Show |
1 | a0001c0002t0001g0159 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1458+5302_1458+530 others(24): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
GTA | G | 44 | a0001c0001t0002g0034a0001c0001t0002g0055a0001c0001t0002g0085others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1458+5301_1458+530 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
GTATA | G | 6 | a0001c0001t0002g0206a0001c0001t0002g0335a0001c0001t0017g0018others(3): Show | 7 | HG00609.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1458+5299_1458+530 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524542
|
GTATATAT others(1): Show |
G | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1458+5295_1458+530 others(12): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524542 | ||||||
| chr18:66524544
|
A | G | 20 | a0001c0002t0008g0325a0002c0004t0005g0017a0002c0004t0005g0119others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1458+5301T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524544 | ||||||
| chr18:66524546
|
A | G | 21 | a0001c0001t0004g0075a0001c0001t0014g0076a0002c0004t0005g0017others(18): Show | 21 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1458+5299T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524546 | ||||||
| chr18:66524548
|
A | G | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1458+5297T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524548 | ||||||
| chr18:66524569
|
T | A | 2 | a0001c0002t0001g0159a0001c0002t0001g0222 | 2 | NA18993.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1458+5276A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(1): Show |
3 | a0001c0002t0018g0036a0001c0003t0019g0027a0001c0003t0019g0029 | 3 | HG03225.hp1 NA19074.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1458+5275_1458+527 others(12): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(3): Show |
6 | a0001c0002t0001g0065a0001c0002t0001g0094a0001c0002t0001g0320others(3): Show | 6 | HG00323.hp1 HG00733.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1458+5275_1458+527 others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(5): Show |
13 | a0001c0001t0004g0165a0001c0002t0001g0030a0001c0002t0001g0043others(10): Show | 13 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1458+5275_1458+527 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(7): Show |
26 | a0001c0001t0002g0256a0001c0002t0001g0023a0001c0002t0001g0033others(23): Show | 26 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1458+5275_1458+527 others(18): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(8): Show |
1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1458+5275_1458+527 others(19): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(9): Show |
26 | a0001c0001t0003g0114a0001c0002t0001g0063a0001c0002t0001g0138others(23): Show | 26 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1458+5275_1458+527 others(20): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(11): Show |
13 | a0001c0001t0003g0241a0001c0002t0001g0156a0001c0002t0001g0157others(10): Show | 13 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1458+5275_1458+527 others(22): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(13): Show |
4 | a0001c0002t0001g0129a0001c0002t0001g0234a0001c0003t0004g0297others(1): Show | 4 | HG01981.hp1 HG02523.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.1458+5275_1458+527 others(24): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(15): Show |
3 | a0001c0001t0003g0345a0001c0002t0001g0162a0001c0002t0008g0196 | 3 | HG00140.hp1 NA18969.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1458+5275_1458+527 others(26): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524569
|
T | TATATATA others(19): Show |
1 | a0001c0003t0004g0349 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1458+5275_1458+527 others(30): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524569 | ||||||
| chr18:66524570
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0141 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1458+5274_1458+527 others(19): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524570 | ||||||
| chr18:66524570
|
A | ATATATAT others(14): Show |
1 | a0001c0002t0008g0325 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1458+5274_1458+527 others(25): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524570 | ||||||
| chr18:66524571
|
A | T | 1 | a0001c0002t0001g0323 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1458+5274T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524571 | ||||||
| chr18:66524615
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+5230A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524615 | ||||||
| chr18:66524659
|
G | A | 117 | a0001c0001t0002g0256a0001c0001t0003g0114a0001c0001t0003g0241others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1458+5186C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524659 | ||||||
| chr18:66524746
|
T | C | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1458+5099A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524746 | ||||||
| chr18:66524880
|
G | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1458+4965C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66524880 | ||||||
| chr18:66525055
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+4790C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66525055 | ||||||
| chr18:66525104
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+4741C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66525104 | ||||||
| chr18:66525417
|
G | C | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1458+4428C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66525417 | ||||||
| chr18:66525639
|
A | C | 1 | a0001c0001t0003g0345 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1458+4206T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66525639 | ||||||
| chr18:66525785
|
G | A | 1 | a0002c0004t0012g0245 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1458+4060C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66525785 | ||||||
| chr18:66525851
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+3994A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66525851 | ||||||
| chr18:66525926
|
T | C | 56 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(53): Show | 56 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1458+3919A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66525926 | ||||||
| chr18:66526159
|
C | T | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1458+3686G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526159 | ||||||
| chr18:66526172
|
A | T | 1 | a0001c0003t0004g0019 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1458+3673T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526172 | ||||||
| chr18:66526187
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+3658C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526187 | ||||||
| chr18:66526337
|
C | A | 4 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1458+3508G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526337 | ||||||
| chr18:66526426
|
T | A | 1 | a0002c0004t0005g0285 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1458+3419A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526426 | ||||||
| chr18:66526471
|
G | T | 2 | a0001c0001t0027g0180a0001c0003t0002g0008 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1458+3374C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526471 | ||||||
| chr18:66526560
|
T | A | 22 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0009g0116others(19): Show | 23 | HG01255.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1458+3285A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526560 | ||||||
| chr18:66526688
|
A | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+3157T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526688 | ||||||
| chr18:66526835
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1458+3010A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66526835 | ||||||
| chr18:66527045
|
ATATG | A | 15 | a0001c0001t0009g0146a0001c0001t0009g0219a0001c0001t0010g0012others(12): Show | 15 | HG01255.hp2 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1458+2796_1458+279 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527045 | ||||||
| chr18:66527047
|
A | ATG | 118 | a0001c0001t0002g0088a0001c0001t0002g0221a0001c0001t0002g0256others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1458+2796_1458+279 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527047 | ||||||
| chr18:66527047
|
A | ATGTG | 4 | a0001c0002t0001g0320a0001c0002t0001g0326a0001c0003t0004g0185others(1): Show | 4 | HG00733.hp2 HG00741.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1458+2794_1458+279 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527047 | ||||||
| chr18:66527047
|
A | G | 2 | a0003c0005t0022g0346a0003c0005t0040g0126 | 2 | HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1458+2798T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527047 | ||||||
| chr18:66527047
|
ATG | A | 76 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(73): Show | 77 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1458+2796_1458+279 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527047 | ||||||
| chr18:66527435
|
T | C | 14 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0010g0012others(11): Show | 15 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1458+2410A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527435 | ||||||
| chr18:66527492
|
C | T | 13 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(10): Show | 13 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1458+2353G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527492 | ||||||
| chr18:66527563
|
A | G | 1 | a0001c0002t0001g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1458+2282T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527563 | ||||||
| chr18:66527623
|
G | C | 1 | a0003c0005t0043g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1458+2222C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527623 | ||||||
| chr18:66527662
|
A | C | 1 | a0001c0002t0025g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1458+2183T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527662 | ||||||
| chr18:66527752
|
C | CTA | 122 | a0001c0001t0002g0256a0001c0001t0003g0114a0001c0001t0003g0241others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1458+2091_1458+209 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527752 | ||||||
| chr18:66527767
|
A | T | 2 | a0001c0001t0035g0172a0001c0002t0001g0293 | 2 | HG02965.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1458+2078T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527767 | ||||||
| chr18:66527849
|
A | C | 1 | a0001c0001t0003g0232 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1458+1996T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527849 | ||||||
| chr18:66527853
|
AT | A | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1458+1991delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66527853 | ||||||
| chr18:66528025
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1458+1820A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528025 | ||||||
| chr18:66528152
|
T | C | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1458+1693A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528152 | ||||||
| chr18:66528187
|
A | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1458+1658T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528187 | ||||||
| chr18:66528360
|
C | T | 1 | a0001c0001t0011g0014 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1458+1485G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528360 | ||||||
| chr18:66528364
|
T | C | 3 | a0005c0009t0011g0025a0005c0009t0011g0247a0005c0009t0011g0248 | 3 | HG02559.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1458+1481A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528364 | ||||||
| chr18:66528373
|
C | T | 99 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(96): Show | 100 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.1458+1472G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528373 | ||||||
| chr18:66528402
|
G | T | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1458+1443C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528402 | ||||||
| chr18:66528451
|
C | T | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1458+1394G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528451 | ||||||
| chr18:66528502
|
C | T | 13 | a0001c0001t0002g0034a0001c0001t0002g0085a0001c0001t0002g0087others(10): Show | 13 | HG02132.hp1 HG03927.hp1 NA18964.hp2 others(10): Show |
intron_variant | MODIFIER | c.1458+1343G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528502 | ||||||
| chr18:66528631
|
G | C | 118 | a0001c0001t0002g0256a0001c0001t0003g0114a0001c0001t0003g0241others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1458+1214C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528631 | ||||||
| chr18:66528643
|
T | TCA | 99 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(96): Show | 100 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.1458+1200_1458+120 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528643 | ||||||
| chr18:66528711
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1458+1134C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528711 | ||||||
| chr18:66528848
|
T | TTGATAA | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1458+991_1458+996d others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66528848 | ||||||
| chr18:66529001
|
A | AAGACAGC others(27): Show |
1 | a0001c0001t0003g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1458+843_1458+844i others(36): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66529001 | ||||||
| chr18:66529284
|
T | C | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1458+561A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66529284 | ||||||
| chr18:66529566
|
GTAAT | G | 115 | a0001c0001t0002g0256a0001c0001t0003g0114a0001c0001t0003g0241others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.1458+275_1458+278d others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66529566 | ||||||
| chr18:66529589
|
T | A | 2 | a0001c0001t0002g0226a0001c0001t0002g0312 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1458+256A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66529589 | ||||||
| chr18:66529597
|
T | A | 6 | a0001c0001t0002g0274a0001c0001t0023g0190a0004c0006t0004g0024others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1458+248A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 9/11 | chr18 | 66529597 | ||||||
| chr18:66529999
|
CAT | C | 22 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0009g0116others(19): Show | 23 | HG01255.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1337-35_1337-34del others(2): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66529999 | ||||||
| chr18:66530052
|
C | T | 10 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0010g0012others(7): Show | 10 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337-86G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530052 | ||||||
| chr18:66530059
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337-93A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530059 | ||||||
| chr18:66530077
|
A | G | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1337-111T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530077 | ||||||
| chr18:66530153
|
C | T | 2 | a0001c0001t0002g0102a0001c0001t0006g0103 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1337-187G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530153 | ||||||
| chr18:66530179
|
T | G | 6 | a0002c0004t0005g0275a0002c0004t0005g0276a0002c0004t0005g0277others(3): Show | 6 | HG01070.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1337-213A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530179 | ||||||
| chr18:66530261
|
C | T | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | NA18966.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1337-295G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530261 | ||||||
| chr18:66530338
|
T | A | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1337-372A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530338 | ||||||
| chr18:66530376
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1337-410A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530376 | ||||||
| chr18:66530408
|
T | C | 7 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337-442A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530408 | ||||||
| chr18:66530469
|
C | T | 1 | a0001c0001t0044g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1337-503G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530469 | ||||||
| chr18:66530583
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337-617C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530583 | ||||||
| chr18:66530653
|
T | TA | 219 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1337-688dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530653 | ||||||
| chr18:66530681
|
A | C | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1337-715T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530681 | ||||||
| chr18:66530774
|
G | A | 1 | a0001c0001t0015g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1337-808C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530774 | ||||||
| chr18:66530912
|
A | G | 1 | a0001c0001t0009g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1337-946T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530912 | ||||||
| chr18:66530958
|
C | T | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1337-992G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66530958 | ||||||
| chr18:66531046
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337-1080C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531046 | ||||||
| chr18:66531161
|
A | G | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1337-1195T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531161 | ||||||
| chr18:66531210
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1337-1244G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531210 | ||||||
| chr18:66531324
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1337-1358A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531324 | ||||||
| chr18:66531353
|
C | T | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337-1387G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531353 | ||||||
| chr18:66531482
|
A | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337-1516T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531482 | ||||||
| chr18:66531536
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337-1570A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531536 | ||||||
| chr18:66531723
|
C | G | 1 | a0001c0003t0004g0143 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1337-1757G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531723 | ||||||
| chr18:66531827
|
A | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1337-1861T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531827 | ||||||
| chr18:66531977
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1337-2011C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66531977 | ||||||
| chr18:66532078
|
T | C | 4 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1337-2112A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532078 | ||||||
| chr18:66532278
|
T | TA | 76 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(73): Show | 77 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1337-2313dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532278 | ||||||
| chr18:66532310
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337-2344A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532310 | ||||||
| chr18:66532385
|
A | G | 1 | a0001c0003t0004g0349 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1337-2419T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532385 | ||||||
| chr18:66532471
|
C | T | 1 | a0001c0002t0008g0198 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1337-2505G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532471 | ||||||
| chr18:66532489
|
T | TAC | 22 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(19): Show | 22 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1336+2495_1336+249 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACAC | 4 | a0001c0001t0002g0254a0001c0001t0003g0123a0001c0001t0003g0131others(1): Show | 4 | HG01934.hp1 HG02615.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336+2493_1336+249 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACAC | 7 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336+2491_1336+249 others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(1): Show |
4 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0037g0212others(1): Show | 4 | HG02109.hp1 HG02809.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336+2489_1336+249 others(12): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(3): Show |
42 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(39): Show | 42 | HG00673.hp1 HG00735.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1336+2487_1336+249 others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(5): Show |
9 | a0001c0001t0002g0133a0001c0001t0004g0107a0001c0001t0006g0013others(6): Show | 9 | HG00642.hp2 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1336+2485_1336+249 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(7): Show |
5 | a0001c0001t0017g0137a0001c0001t0023g0190a0001c0002t0001g0201others(2): Show | 5 | HG02451.hp1 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336+2483_1336+249 others(18): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(9): Show |
2 | a0001c0001t0002g0274a0004c0006t0014g0235 | 2 | HG01109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1336+2481_1336+249 others(20): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(11): Show |
6 | a0001c0001t0011g0347a0001c0001t0020g0001a0001c0001t0027g0180others(3): Show | 7 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1336+2479_1336+249 others(22): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(13): Show |
3 | a0001c0001t0017g0018a0001c0001t0017g0182a0005c0009t0011g0025 | 3 | HG02559.hp1 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1336+2477_1336+249 others(24): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(15): Show |
2 | a0001c0001t0011g0236a0005c0009t0011g0247 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1336+2475_1336+249 others(26): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(17): Show |
2 | a0001c0001t0011g0014a0005c0009t0011g0248 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1336+2473_1336+249 others(28): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACACA others(19): Show |
1 | a0001c0001t0011g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1336+2471_1336+249 others(30): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACTCA others(3): Show |
2 | a0003c0005t0022g0346a0003c0005t0040g0126 | 2 | HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1336+2496_1336+249 others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACTCA others(5): Show |
1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1336+2496_1336+249 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACTCA others(7): Show |
6 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336+2496_1336+249 others(18): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532489
|
T | TACACTCA others(9): Show |
1 | a0003c0005t0026g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1336+2496_1336+249 others(20): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532489 | ||||||
| chr18:66532719
|
G | T | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336+2267C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532719 | ||||||
| chr18:66532841
|
C | T | 1 | a0001c0003t0004g0171 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1336+2145G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532841 | ||||||
| chr18:66532947
|
ATATT | A | 6 | a0001c0001t0002g0274a0001c0001t0023g0190a0004c0006t0004g0024others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336+2035_1336+203 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66532947 | ||||||
| chr18:66533024
|
A | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1336+1962T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533024 | ||||||
| chr18:66533178
|
T | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336+1808A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533178 | ||||||
| chr18:66533213
|
T | TAC | 35 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(32): Show | 35 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.1336+1771_1336+177 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533213 | ||||||
| chr18:66533213
|
T | TACAC | 22 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(19): Show | 22 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1336+1769_1336+177 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533213 | ||||||
| chr18:66533213
|
T | TACACAC | 3 | a0001c0001t0006g0111a0002c0004t0012g0238a0003c0005t0026g0010 | 3 | HG01952.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1336+1767_1336+177 others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533213 | ||||||
| chr18:66533213
|
T | TACACACA others(3): Show |
6 | a0001c0001t0009g0146a0001c0001t0009g0219a0001c0001t0035g0172others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336+1763_1336+177 others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533213 | ||||||
| chr18:66533213
|
T | TACACACA others(5): Show |
1 | a0001c0001t0009g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1336+1761_1336+177 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533213 | ||||||
| chr18:66533213
|
TAC | T | 129 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0256others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1336+1771_1336+177 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533213 | ||||||
| chr18:66533221
|
C | T | 1 | a0001c0001t0017g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1336+1765G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533221 | ||||||
| chr18:66533233
|
C | T | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1336+1753G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533233 | ||||||
| chr18:66533235
|
C | T | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336+1751G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533235 | ||||||
| chr18:66533292
|
T | G | 1 | a0001c0002t0001g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1336+1694A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533292 | ||||||
| chr18:66533421
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336+1565C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533421 | ||||||
| chr18:66533625
|
A | ATAGT | 218 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1336+1357_1336+136 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533625 | ||||||
| chr18:66533738
|
A | T | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336+1248T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66533738 | ||||||
| chr18:66534016
|
A | T | 2 | a0005c0009t0011g0025a0005c0009t0011g0247 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1336+970T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534016 | ||||||
| chr18:66534060
|
T | C | 1 | a0001c0001t0003g0324 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1336+926A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534060 | ||||||
| chr18:66534063
|
T | C | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1336+923A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534063 | ||||||
| chr18:66534097
|
G | GA | 8 | a0001c0001t0027g0180a0001c0002t0001g0262a0001c0002t0008g0325others(5): Show | 8 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1336+888dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534097 | ||||||
| chr18:66534097
|
GA | G | 16 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0009g0130others(13): Show | 16 | HG00621.hp1 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1336+888delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534097 | ||||||
| chr18:66534123
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1336+863T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534123 | ||||||
| chr18:66534126
|
C | A | 5 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336+860G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534126 | ||||||
| chr18:66534272
|
A | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336+714T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534272 | ||||||
| chr18:66534318
|
C | T | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1336+668G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534318 | ||||||
| chr18:66534436
|
G | T | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336+550C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534436 | ||||||
| chr18:66534454
|
G | T | 1 | a0001c0001t0032g0200 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1336+532C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534454 | ||||||
| chr18:66534556
|
C | T | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1336+430G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534556 | ||||||
| chr18:66534619
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336+367A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534619 | ||||||
| chr18:66534834
|
C | T | 1 | a0001c0001t0009g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1336+152G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534834 | ||||||
| chr18:66534897
|
T | A | 1 | a0001c0002t0001g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1336+89A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 8/11 | chr18 | 66534897 | ||||||
| chr18:66535146
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215-39A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535146 | ||||||
| chr18:66535148
|
T | C | 1 | a0001c0003t0004g0296 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1215-41A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535148 | ||||||
| chr18:66535149
|
C | G | 2 | a0001c0003t0004g0132a0001c0003t0004g0220 | 2 | NA18939.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1215-42G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535149 | ||||||
| chr18:66535209
|
C | G | 1 | a0001c0002t0001g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1215-102G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535209 | ||||||
| chr18:66535259
|
G | A | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1215-152C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535259 | ||||||
| chr18:66535314
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215-207A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535314 | ||||||
| chr18:66535348
|
A | G | 1 | a0001c0001t0003g0328 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1215-241T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535348 | ||||||
| chr18:66535362
|
T | C | 42 | a0001c0001t0002g0256a0001c0002t0001g0094a0001c0002t0001g0174others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.1215-255A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535362 | ||||||
| chr18:66535401
|
C | T | 80 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(77): Show | 81 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1215-294G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535401 | ||||||
| chr18:66535419
|
C | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1215-312G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535419 | ||||||
| chr18:66535440
|
C | T | 7 | a0001c0001t0003g0064a0001c0001t0003g0230a0001c0001t0003g0271others(4): Show | 7 | HG00735.hp2 HG01109.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215-333G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535440 | ||||||
| chr18:66535467
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1215-360A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535467 | ||||||
| chr18:66535496
|
T | C | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215-389A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535496 | ||||||
| chr18:66535544
|
G | A | 5 | a0001c0002t0001g0094a0001c0002t0001g0244a0001c0002t0001g0286others(2): Show | 5 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215-437C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535544 | ||||||
| chr18:66535615
|
T | TTA | 9 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1215-510_1215-509d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535615 | ||||||
| chr18:66535617
|
A | T | 17 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(14): Show | 17 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1215-510T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535617 | ||||||
| chr18:66535645
|
A | G | 4 | a0001c0001t0002g0087a0001c0001t0002g0089a0001c0001t0002g0224others(1): Show | 4 | HG02132.hp1 HG03927.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215-538T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535645 | ||||||
| chr18:66535666
|
A | G | 3 | a0001c0003t0004g0039a0001c0003t0004g0267a0001c0003t0004g0269 | 3 | NA18945.hp2 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1215-559T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535666 | ||||||
| chr18:66535699
|
T | C | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1215-592A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535699 | ||||||
| chr18:66535746
|
T | C | 5 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215-639A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535746 | ||||||
| chr18:66535780
|
CAT | C | 8 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1215-675_1215-674d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535780 | ||||||
| chr18:66535817
|
CAT | C | 46 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(43): Show | 46 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1215-712_1215-711d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535817 | ||||||
| chr18:66535828
|
T | A | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215-721A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535828 | ||||||
| chr18:66535896
|
A | G | 7 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215-789T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66535896 | ||||||
| chr18:66536028
|
AG | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215-922delC | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536028 | ||||||
| chr18:66536031
|
G | A | 209 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1215-924C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536031 | ||||||
| chr18:66536082
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215-975C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536082 | ||||||
| chr18:66536098
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1215-991G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536098 | ||||||
| chr18:66536138
|
C | T | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215-1031G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536138 | ||||||
| chr18:66536163
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215-1056C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536163 | ||||||
| chr18:66536295
|
C | A | 1 | a0001c0001t0023g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1215-1188G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536295 | ||||||
| chr18:66536337
|
A | G | 9 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0083others(6): Show | 9 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1215-1230T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536337 | ||||||
| chr18:66536488
|
T | A | 1 | a0001c0003t0004g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1215-1381A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536488 | ||||||
| chr18:66536576
|
T | C | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1215-1469A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536576 | ||||||
| chr18:66536585
|
A | G | 1 | a0001c0001t0003g0338 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1215-1478T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536585 | ||||||
| chr18:66536679
|
T | C | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1215-1572A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536679 | ||||||
| chr18:66536776
|
T | G | 14 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(11): Show | 15 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1215-1669A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536776 | ||||||
| chr18:66536781
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1215-1674A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536781 | ||||||
| chr18:66536851
|
A | T | 9 | a0001c0001t0002g0208a0001c0001t0004g0209a0001c0001t0011g0014others(6): Show | 9 | HG01891.hp2 HG02559.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215-1744T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536851 | ||||||
| chr18:66536903
|
G | A | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1215-1796C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536903 | ||||||
| chr18:66536931
|
C | A | 3 | a0002c0004t0005g0128a0002c0004t0005g0329a0002c0004t0012g0238 | 3 | HG01952.hp1 HG01981.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1215-1824G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66536931 | ||||||
| chr18:66537116
|
T | C | 121 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0256others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1215-2009A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66537116 | ||||||
| chr18:66537118
|
G | A | 4 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0017g0182others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215-2011C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66537118 | ||||||
| chr18:66537215
|
C | T | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1215-2108G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66537215 | ||||||
| chr18:66537331
|
A | G | 1 | a0002c0004t0005g0017 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1215-2224T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66537331 | ||||||
| chr18:66537441
|
T | G | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1215-2334A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66537441 | ||||||
| chr18:66537498
|
C | T | 46 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(43): Show | 46 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1215-2391G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66537498 | ||||||
| chr18:66537635
|
A | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215-2528T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66537635 | ||||||
| chr18:66537772
|
C | T | 2 | a0001c0001t0027g0180a0001c0003t0002g0008 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1215-2665G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66537772 | ||||||
| chr18:66538059
|
T | C | 19 | a0001c0001t0002g0274a0001c0001t0009g0130a0001c0001t0009g0146others(16): Show | 19 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1215-2952A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538059 | ||||||
| chr18:66538213
|
G | T | 9 | a0001c0001t0002g0274a0001c0001t0023g0190a0004c0006t0004g0024others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1215-3106C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538213 | ||||||
| chr18:66538413
|
C | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1215-3306G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538413 | ||||||
| chr18:66538490
|
G | A | 46 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(43): Show | 46 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1215-3383C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538490 | ||||||
| chr18:66538491
|
G | T | 2 | a0001c0001t0002g0088a0001c0001t0002g0221 | 2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1215-3384C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538491 | ||||||
| chr18:66538543
|
T | C | 16 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0010g0012others(13): Show | 17 | HG01255.hp2 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1215-3436A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538543 | ||||||
| chr18:66538571
|
T | C | 1 | a0001c0001t0007g0047 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1215-3464A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538571 | ||||||
| chr18:66538602
|
G | C | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1215-3495C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538602 | ||||||
| chr18:66538603
|
G | A | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1215-3496C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538603 | ||||||
| chr18:66538635
|
C | T | 1 | a0001c0001t0009g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1215-3528G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538635 | ||||||
| chr18:66538654
|
A | G | 46 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(43): Show | 46 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1215-3547T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538654 | ||||||
| chr18:66538809
|
A | G | 19 | a0001c0001t0002g0274a0001c0001t0009g0130a0001c0001t0009g0146others(16): Show | 19 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1215-3702T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538809 | ||||||
| chr18:66538889
|
A | G | 1 | a0007c0012t0021g0090 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1215-3782T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538889 | ||||||
| chr18:66538919
|
C | G | 3 | a0001c0001t0013g0022a0001c0001t0013g0217a0001c0001t0013g0225 | 3 | HG02145.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1215-3812G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66538919 | ||||||
| chr18:66539152
|
C | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1215-4045G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539152 | ||||||
| chr18:66539197
|
G | A | 2 | a0002c0004t0012g0282a0002c0004t0028g0178 | 2 | HG00642.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1215-4090C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539197 | ||||||
| chr18:66539519
|
A | G | 2 | a0001c0001t0027g0180a0001c0003t0002g0008 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1215-4412T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539519 | ||||||
| chr18:66539526
|
T | G | 46 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(43): Show | 46 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1215-4419A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539526 | ||||||
| chr18:66539553
|
C | G | 19 | a0001c0001t0002g0274a0001c0001t0009g0130a0001c0001t0009g0146others(16): Show | 19 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1214+4418G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539553 | ||||||
| chr18:66539635
|
A | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1214+4336T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539635 | ||||||
| chr18:66539735
|
G | A | 2 | a0001c0001t0027g0180a0001c0003t0002g0008 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1214+4236C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539735 | ||||||
| chr18:66539780
|
C | CT | 19 | a0001c0001t0002g0274a0001c0001t0009g0130a0001c0001t0009g0146others(16): Show | 19 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1214+4190dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539780 | ||||||
| chr18:66539831
|
T | C | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214+4140A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539831 | ||||||
| chr18:66539844
|
G | A | 19 | a0001c0001t0002g0274a0001c0001t0009g0130a0001c0001t0009g0146others(16): Show | 19 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1214+4127C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539844 | ||||||
| chr18:66539894
|
A | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1214+4077T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66539894 | ||||||
| chr18:66540199
|
C | A | 1 | a0001c0001t0016g0327 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1214+3772G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66540199 | ||||||
| chr18:66540449
|
C | G | 119 | a0001c0001t0002g0256a0001c0001t0003g0114a0001c0001t0003g0241others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1214+3522G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66540449 | ||||||
| chr18:66540508
|
C | T | 1 | a0001c0001t0002g0335 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1214+3463G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66540508 | ||||||
| chr18:66540652
|
G | A | 1 | a0001c0002t0001g0323 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1214+3319C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66540652 | ||||||
| chr18:66540663
|
C | T | 1 | a0001c0001t0003g0336 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1214+3308G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66540663 | ||||||
| chr18:66540824
|
G | A | 1 | a0001c0001t0015g0237 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1214+3147C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66540824 | ||||||
| chr18:66540917
|
G | A | 1 | a0001c0001t0010g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1214+3054C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66540917 | ||||||
| chr18:66541053
|
T | G | 80 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(77): Show | 81 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1214+2918A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66541053 | ||||||
| chr18:66541111
|
A | G | 1 | a0001c0002t0008g0198 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1214+2860T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66541111 | ||||||
| chr18:66541139
|
G | A | 1 | a0001c0001t0004g0344 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1214+2832C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66541139 | ||||||
| chr18:66541153
|
T | C | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1214+2818A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66541153 | ||||||
| chr18:66541347
|
A | AT | 53 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(50): Show | 53 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1214+2623dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66541347 | ||||||
| chr18:66541511
|
C | A | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1214+2460G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66541511 | ||||||
| chr18:66541876
|
T | C | 220 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1214+2095A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66541876 | ||||||
| chr18:66541938
|
A | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1214+2033T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66541938 | ||||||
| chr18:66542233
|
G | T | 1 | a0001c0003t0004g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1214+1738C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66542233 | ||||||
| chr18:66542318
|
T | C | 1 | a0001c0001t0003g0300 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1214+1653A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66542318 | ||||||
| chr18:66542332
|
C | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1214+1639G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66542332 | ||||||
| chr18:66542686
|
C | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1214+1285G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66542686 | ||||||
| chr18:66542788
|
T | C | 1 | a0001c0002t0001g0142 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1214+1183A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66542788 | ||||||
| chr18:66542936
|
G | T | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214+1035C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66542936 | ||||||
| chr18:66542965
|
C | G | 46 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(43): Show | 46 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1214+1006G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66542965 | ||||||
| chr18:66543053
|
T | C | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1214+918A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543053 | ||||||
| chr18:66543172
|
C | G | 1 | a0001c0003t0014g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1214+799G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543172 | ||||||
| chr18:66543220
|
G | A | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214+751C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543220 | ||||||
| chr18:66543230
|
T | G | 1 | a0001c0001t0002g0352 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1214+741A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543230 | ||||||
| chr18:66543249
|
G | A | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1214+722C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543249 | ||||||
| chr18:66543270
|
G | A | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(44): Show | 47 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1214+701C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543270 | ||||||
| chr18:66543339
|
C | T | 77 | a0001c0001t0002g0034a0001c0001t0002g0044a0001c0001t0002g0051others(74): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1214+632G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543339 | ||||||
| chr18:66543457
|
G | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1214+514C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543457 | ||||||
| chr18:66543486
|
C | A | 1 | a0001c0008t0003g0304 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1214+485G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543486 | ||||||
| chr18:66543488
|
A | AT | 3 | a0001c0001t0004g0165a0001c0002t0001g0142a0001c0002t0001g0320 | 3 | HG00733.hp1 HG00733.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1214+482dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543488 | ||||||
| chr18:66543511
|
C | T | 219 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(216): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1214+460G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543511 | ||||||
| chr18:66543610
|
G | A | 1 | a0001c0002t0001g0074 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1214+361C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543610 | ||||||
| chr18:66543739
|
T | C | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1214+232A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543739 | ||||||
| chr18:66543831
|
T | C | 93 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(90): Show | 94 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.1214+140A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543831 | ||||||
| chr18:66543852
|
G | T | 1 | a0001c0001t0003g0070 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1214+119C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543852 | ||||||
| chr18:66543895
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1214+76C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 7/11 | chr18 | 66543895 | ||||||
| chr18:66544299
|
C | T | 3 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0020g0001 | 4 | HG02886.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-75G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 6/11 | chr18 | 66544299 | ||||||
| chr18:66544325
|
TCA | T | 10 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0010g0012others(7): Show | 10 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-103_961-102del others(2): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 6/11 | chr18 | 66544325 | ||||||
| chr18:66544443
|
T | A | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.961-219A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 6/11 | chr18 | 66544443 | ||||||
| chr18:66544482
|
C | CAGTTTTT others(7): Show |
1 | a0001c0001t0027g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.960+236_960+237ins others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 6/11 | chr18 | 66544482 | ||||||
| chr18:66544682
|
C | T | 7 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+37G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 6/11 | chr18 | 66544682 | ||||||
| chr18:66545095
|
C | T | 2 | a0001c0001t0002g0034a0001c0001t0007g0268 | 2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.776-192G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545095 | ||||||
| chr18:66545189
|
A | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.776-286T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545189 | ||||||
| chr18:66545323
|
C | T | 51 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(48): Show | 51 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.776-420G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545323 | ||||||
| chr18:66545393
|
TTTCTTTC others(13): Show |
T | 29 | a0001c0001t0002g0026a0001c0001t0002g0274a0001c0001t0006g0073others(26): Show | 30 | HG01109.hp1 HG01255.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.776-510_776-491del others(20): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545393 | ||||||
| chr18:66545402
|
T | G | 1 | a0001c0001t0004g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.776-499A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545402 | ||||||
| chr18:66545413
|
C | T | 118 | a0001c0001t0002g0256a0001c0001t0003g0114a0001c0001t0003g0241others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.776-510G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545413 | ||||||
| chr18:66545413
|
CTTCT | C | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.776-514_776-511del others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545413 | ||||||
| chr18:66545449
|
A | G | 1 | a0001c0001t0002g0068 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.776-546T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545449 | ||||||
| chr18:66545452
|
C | T | 3 | a0001c0001t0004g0075a0001c0001t0004g0344a0001c0001t0014g0076 | 3 | HG01257.hp2 HG01258.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.776-549G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545452 | ||||||
| chr18:66545535
|
A | C | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.776-632T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545535 | ||||||
| chr18:66545786
|
C | T | 219 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(216): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.776-883G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545786 | ||||||
| chr18:66545802
|
G | A | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.776-899C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545802 | ||||||
| chr18:66545831
|
T | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.776-928A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545831 | ||||||
| chr18:66545948
|
C | CT | 199 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(196): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.776-1046dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66545948 | ||||||
| chr18:66546167
|
T | C | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.776-1264A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546167 | ||||||
| chr18:66546204
|
T | C | 4 | a0001c0001t0003g0064a0005c0009t0011g0025a0005c0009t0011g0247others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.776-1301A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546204 | ||||||
| chr18:66546652
|
G | A | 2 | a0001c0002t0001g0063a0001c0002t0001g0161 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.776-1749C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546652 | ||||||
| chr18:66546654
|
C | G | 1 | a0001c0001t0010g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.776-1751G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546654 | ||||||
| chr18:66546701
|
G | A | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.776-1798C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546701 | ||||||
| chr18:66546819
|
G | A | 2 | a0001c0001t0003g0002a0001c0001t0007g0047 | 3 | NA19068.hp1 NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.776-1916C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546819 | ||||||
| chr18:66546844
|
G | GAGA | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.776-1942_776-1941i others(5): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546844 | ||||||
| chr18:66546856
|
C | G | 1 | a0001c0001t0002g0351 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.776-1953G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546856 | ||||||
| chr18:66546902
|
G | T | 8 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(5): Show | 8 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.776-1999C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66546902 | ||||||
| chr18:66547039
|
G | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.776-2136C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547039 | ||||||
| chr18:66547101
|
G | A | 1 | a0001c0001t0027g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.776-2198C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547101 | ||||||
| chr18:66547177
|
T | A | 4 | a0001c0001t0002g0085a0001c0001t0002g0288a0001c0001t0002g0309others(1): Show | 4 | NA18968.hp2 NA18978.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-2274A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547177 | ||||||
| chr18:66547216
|
A | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.776-2313T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547216 | ||||||
| chr18:66547309
|
G | A | 1 | a0001c0002t0001g0326 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.776-2406C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547309 | ||||||
| chr18:66547382
|
C | G | 1 | a0001c0002t0001g0273 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.776-2479G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547382 | ||||||
| chr18:66547528
|
T | A | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.776-2625A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547528 | ||||||
| chr18:66547557
|
C | T | 4 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-2654G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547557 | ||||||
| chr18:66547657
|
TTAGGTTT others(302): Show |
T | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.776-3063_776-2755d others(2): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547657 | ||||||
| chr18:66547659
|
A | C | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.776-2756T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547659 | ||||||
| chr18:66547661
|
G | GT | 121 | a0001c0001t0002g0068a0001c0001t0002g0083a0001c0001t0002g0203others(118): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.776-2759dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547661 | ||||||
| chr18:66547661
|
G | GTT | 36 | a0001c0001t0003g0324a0001c0001t0003g0328a0001c0001t0003g0338others(33): Show | 36 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.776-2760_776-2759d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547661 | ||||||
| chr18:66547661
|
GT | G | 34 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0101others(31): Show | 34 | HG00673.hp1 HG00735.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.776-2759delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547661 | ||||||
| chr18:66547730
|
G | A | 1 | a0001c0002t0001g0142 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.776-2827C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547730 | ||||||
| chr18:66547731
|
G | C | 1 | a0001c0001t0009g0322 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.776-2828C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547731 | ||||||
| chr18:66547775
|
C | T | 1 | a0001c0003t0004g0184 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.776-2872G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547775 | ||||||
| chr18:66547822
|
T | C | 1 | a0001c0001t0004g0007 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.776-2919A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547822 | ||||||
| chr18:66547871
|
T | G | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.776-2968A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547871 | ||||||
| chr18:66547894
|
C | T | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.776-2991G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547894 | ||||||
| chr18:66547911
|
C | T | 1 | a0001c0001t0003g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.776-3008G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66547911 | ||||||
| chr18:66548125
|
TA | T | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.775+2968delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548125 | ||||||
| chr18:66548129
|
A | T | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.775+2965T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548129 | ||||||
| chr18:66548245
|
TTA | T | 11 | a0001c0001t0002g0226a0001c0001t0002g0312a0001c0002t0001g0120others(8): Show | 11 | HG01070.hp1 HG02258.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.775+2847_775+2848d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548245 | ||||||
| chr18:66548257
|
A | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.775+2837T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548257 | ||||||
| chr18:66548258
|
TA | T | 173 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.775+2835delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548258 | ||||||
| chr18:66548259
|
A | T | 16 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(13): Show | 16 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.775+2835T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548259 | ||||||
| chr18:66548260
|
TA | T | 7 | a0001c0002t0001g0273a0001c0003t0002g0008a0002c0004t0005g0017others(4): Show | 7 | HG00735.hp1 HG02559.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+2833delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548260 | ||||||
| chr18:66548261
|
A | T | 208 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.775+2833T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548261 | ||||||
| chr18:66548261
|
AT | A | 5 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+2832delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548261 | ||||||
| chr18:66548263
|
T | A | 2 | a0001c0001t0003g0249a0001c0001t0015g0246 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.775+2831A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548263 | ||||||
| chr18:66548266
|
T | A | 20 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0010g0012others(17): Show | 21 | HG01255.hp2 HG02080.hp1 HG02155.hp2 others(18): Show |
intron_variant | MODIFIER | c.775+2828A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548266 | ||||||
| chr18:66548267
|
T | A | 102 | a0001c0001t0002g0026a0001c0001t0002g0135a0001c0001t0002g0136others(99): Show | 103 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.775+2827A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548267 | ||||||
| chr18:66548268
|
T | A | 158 | a0001c0001t0002g0026a0001c0001t0002g0135a0001c0001t0002g0136others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.775+2826A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548268 | ||||||
| chr18:66548268
|
TA | T | 16 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(13): Show | 16 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.775+2825delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548268 | ||||||
| chr18:66548269
|
A | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(8): Show | 11 | HG00735.hp1 HG02056.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.775+2825T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548269 | ||||||
| chr18:66548270
|
A | T | 1 | a0003c0005t0026g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.775+2824T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548270 | ||||||
| chr18:66548376
|
G | C | 2 | a0001c0003t0004g0152a0001c0003t0014g0041 | 2 | NA18747.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.775+2718C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548376 | ||||||
| chr18:66548382
|
GT | G | 220 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.775+2711delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548382 | ||||||
| chr18:66548475
|
G | A | 1 | a0001c0001t0013g0069 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.775+2619C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548475 | ||||||
| chr18:66548482
|
A | T | 1 | a0001c0001t0038g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.775+2612T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548482 | ||||||
| chr18:66548491
|
A | AAAGAAG | 220 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.775+2602_775+2603i others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548491 | ||||||
| chr18:66548578
|
A | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.775+2516T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548578 | ||||||
| chr18:66548650
|
C | T | 220 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.775+2444G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548650 | ||||||
| chr18:66548875
|
G | C | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.775+2219C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548875 | ||||||
| chr18:66548901
|
C | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.775+2193G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548901 | ||||||
| chr18:66548962
|
A | C | 1 | a0001c0003t0004g0197 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.775+2132T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66548962 | ||||||
| chr18:66549028
|
C | A | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.775+2066G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549028 | ||||||
| chr18:66549030
|
T | C | 1 | a0001c0001t0003g0336 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.775+2064A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549030 | ||||||
| chr18:66549126
|
A | G | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(44): Show | 47 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.775+1968T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549126 | ||||||
| chr18:66549427
|
T | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.775+1667A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549427 | ||||||
| chr18:66549553
|
C | T | 2 | a0001c0003t0004g0019a0001c0003t0004g0020 | 2 | NA18952.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.775+1541G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549553 | ||||||
| chr18:66549694
|
G | T | 1 | a0001c0014t0003g0314 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.775+1400C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549694 | ||||||
| chr18:66549740
|
G | T | 1 | a0001c0001t0003g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.775+1354C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549740 | ||||||
| chr18:66549828
|
T | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.775+1266A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549828 | ||||||
| chr18:66549977
|
G | T | 3 | a0005c0009t0011g0025a0005c0009t0011g0247a0005c0009t0011g0248 | 3 | HG02559.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.775+1117C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66549977 | ||||||
| chr18:66550061
|
A | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.775+1033T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550061 | ||||||
| chr18:66550081
|
A | G | 1 | a0002c0004t0005g0285 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.775+1013T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550081 | ||||||
| chr18:66550115
|
A | G | 3 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0020g0001 | 4 | HG02886.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+979T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550115 | ||||||
| chr18:66550158
|
G | C | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.775+936C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550158 | ||||||
| chr18:66550187
|
A | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.775+907T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550187 | ||||||
| chr18:66550265
|
T | G | 1 | a0001c0001t0011g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.775+829A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550265 | ||||||
| chr18:66550410
|
T | A | 4 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+684A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550410 | ||||||
| chr18:66550464
|
G | A | 14 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.775+630C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550464 | ||||||
| chr18:66550481
|
A | T | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.775+613T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550481 | ||||||
| chr18:66550487
|
T | C | 1 | a0001c0010t0001g0308 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.775+607A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550487 | ||||||
| chr18:66550541
|
A | G | 2 | a0002c0004t0005g0119a0002c0004t0005g0298 | 2 | HG03239.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.775+553T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550541 | ||||||
| chr18:66550600
|
G | A | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(23): Show | 26 | HG00735.hp1 HG01884.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.775+494C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550600 | ||||||
| chr18:66550680
|
C | A | 2 | a0001c0002t0001g0311a0001c0002t0001g0317 | 2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.775+414G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 5/11 | chr18 | 66550680 | ||||||
| chr18:66551338
|
A | G | 10 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.611-80T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66551338 | ||||||
| chr18:66551499
|
T | C | 3 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0020g0001 | 4 | HG02886.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-241A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66551499 | ||||||
| chr18:66551545
|
T | C | 13 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0010g0012others(10): Show | 14 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.611-287A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66551545 | ||||||
| chr18:66551602
|
G | A | 2 | a0001c0001t0017g0182a0001c0001t0023g0190 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.611-344C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66551602 | ||||||
| chr18:66551674
|
C | G | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.611-416G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66551674 | ||||||
| chr18:66551764
|
T | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.611-506A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66551764 | ||||||
| chr18:66551797
|
A | C | 1 | a0001c0001t0002g0335 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.611-539T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66551797 | ||||||
| chr18:66551861
|
T | C | 3 | a0001c0001t0010g0139a0001c0001t0010g0251a0001c0001t0024g0003 | 3 | HG01255.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.611-603A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66551861 | ||||||
| chr18:66552167
|
A | T | 1 | a0001c0002t0001g0201 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.611-909T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552167 | ||||||
| chr18:66552197
|
C | T | 5 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-939G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552197 | ||||||
| chr18:66552271
|
T | C | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.611-1013A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552271 | ||||||
| chr18:66552383
|
A | G | 1 | a0001c0003t0004g0218 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.611-1125T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552383 | ||||||
| chr18:66552396
|
G | T | 4 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-1138C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552396 | ||||||
| chr18:66552422
|
TA | T | 80 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(77): Show | 81 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611-1165delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552422 | ||||||
| chr18:66552458
|
G | T | 80 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(77): Show | 81 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611-1200C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552458 | ||||||
| chr18:66552466
|
TGTTTCAC others(1543): Show |
T | 80 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(77): Show | 81 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.610+389_611-1209de others(1): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552466 | ||||||
| chr18:66552482
|
T | C | 1 | a0001c0001t0003g0035 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.611-1224A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552482 | ||||||
| chr18:66552807
|
G | A | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.611-1549C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66552807 | ||||||
| chr18:66553033
|
C | T | 1 | a0001c0011t0002g0306 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.610+1372G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553033 | ||||||
| chr18:66553042
|
T | C | 5 | a0001c0001t0039g0319a0003c0005t0022g0346a0003c0005t0026g0010others(2): Show | 5 | HG01433.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+1363A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553042 | ||||||
| chr18:66553043
|
G | C | 5 | a0001c0001t0039g0319a0003c0005t0022g0346a0003c0005t0026g0010others(2): Show | 5 | HG01433.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+1362C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553043 | ||||||
| chr18:66553069
|
C | A | 2 | a0001c0002t0001g0323a0001c0002t0001g0332 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.610+1336G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553069 | ||||||
| chr18:66553430
|
G | A | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.610+975C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553430 | ||||||
| chr18:66553435
|
T | G | 1 | a0001c0002t0001g0160 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.610+970A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553435 | ||||||
| chr18:66553443
|
T | C | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.610+962A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553443 | ||||||
| chr18:66553546
|
A | C | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.610+859T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553546 | ||||||
| chr18:66553655
|
A | C | 1 | a0001c0001t0009g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.610+750T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553655 | ||||||
| chr18:66553685
|
CTA | C | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.610+718_610+719del others(2): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553685 | ||||||
| chr18:66553995
|
G | C | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.610+410C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66553995 | ||||||
| chr18:66554087
|
T | C | 1 | a0001c0001t0003g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.610+318A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66554087 | ||||||
| chr18:66554136
|
G | C | 1 | a0001c0001t0017g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.610+269C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66554136 | ||||||
| chr18:66554169
|
C | A | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.610+236G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66554169 | ||||||
| chr18:66554174
|
C | T | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.610+231G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 4/11 | chr18 | 66554174 | ||||||
| chr18:66554699
|
C | A | 1 | a0001c0001t0011g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.491-175G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66554699 | ||||||
| chr18:66554732
|
T | C | 1 | a0001c0001t0002g0087 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.491-208A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66554732 | ||||||
| chr18:66554964
|
T | C | 1 | a0001c0001t0013g0069 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.491-440A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66554964 | ||||||
| chr18:66555213
|
T | C | 1 | a0001c0003t0004g0181 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.491-689A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555213 | ||||||
| chr18:66555301
|
G | T | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | NA18966.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.491-777C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555301 | ||||||
| chr18:66555317
|
C | T | 5 | a0001c0003t0004g0132a0001c0003t0004g0169a0001c0003t0004g0197others(2): Show | 5 | HG02080.hp1 HG02602.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-793G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555317 | ||||||
| chr18:66555385
|
A | G | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.491-861T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555385 | ||||||
| chr18:66555390
|
AG | A | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.491-867delC | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555390 | ||||||
| chr18:66555552
|
T | C | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.491-1028A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555552 | ||||||
| chr18:66555680
|
C | T | 4 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(1): Show | 4 | NA18947.hp2 NA18960.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-1156G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555680 | ||||||
| chr18:66555748
|
A | G | 1 | a0002c0004t0012g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.491-1224T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555748 | ||||||
| chr18:66555785
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.491-1261G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555785 | ||||||
| chr18:66555855
|
A | G | 1 | a0001c0001t0002g0215 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.491-1331T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555855 | ||||||
| chr18:66555855
|
AATTCTCT others(3): Show |
A | 1 | a0001c0003t0004g0152 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.491-1341_491-1332d others(12): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66555855 | ||||||
| chr18:66556146
|
T | G | 1 | a0001c0001t0003g0230 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.491-1622A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556146 | ||||||
| chr18:66556148
|
T | A | 8 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(5): Show | 8 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-1624A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556148 | ||||||
| chr18:66556207
|
A | G | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-1683T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556207 | ||||||
| chr18:66556316
|
A | G | 1 | a0003c0005t0040g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.491-1792T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556316 | ||||||
| chr18:66556435
|
T | C | 228 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.491-1911A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556435 | ||||||
| chr18:66556464
|
C | T | 2 | a0001c0001t0003g0348a0001c0001t0032g0200 | 2 | NA19057.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.491-1940G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556464 | ||||||
| chr18:66556506
|
T | G | 8 | a0001c0001t0003g0153a0001c0001t0013g0057a0001c0001t0013g0069others(5): Show | 8 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-1982A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556506 | ||||||
| chr18:66556683
|
T | G | 4 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-2159A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556683 | ||||||
| chr18:66556695
|
C | T | 14 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.491-2171G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556695 | ||||||
| chr18:66556759
|
G | T | 4 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-2235C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556759 | ||||||
| chr18:66556807
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.491-2283A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66556807 | ||||||
| chr18:66557738
|
T | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.491-3214A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66557738 | ||||||
| chr18:66557792
|
T | A | 1 | a0001c0003t0004g0218 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.491-3268A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66557792 | ||||||
| chr18:66557814
|
G | A | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-3290C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66557814 | ||||||
| chr18:66557950
|
G | C | 1 | a0001c0001t0003g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.491-3426C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66557950 | ||||||
| chr18:66558079
|
G | T | 1 | a0001c0001t0002g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.491-3555C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558079 | ||||||
| chr18:66558119
|
G | T | 29 | a0001c0001t0002g0026a0001c0001t0002g0274a0001c0001t0006g0073others(26): Show | 30 | HG01109.hp1 HG01255.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.491-3595C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558119 | ||||||
| chr18:66558156
|
T | A | 228 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.491-3632A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558156 | ||||||
| chr18:66558162
|
C | CAT | 21 | a0001c0003t0002g0008a0002c0004t0005g0017a0002c0004t0005g0119others(18): Show | 21 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.491-3640_491-3639d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558162 | ||||||
| chr18:66558162
|
C | CATAT | 3 | a0001c0001t0017g0018a0001c0001t0017g0137a0001c0001t0020g0001 | 4 | HG02886.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-3642_491-3639d others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558162 | ||||||
| chr18:66558162
|
CAT | C | 15 | a0001c0001t0002g0274a0001c0001t0011g0014a0001c0001t0017g0182others(12): Show | 15 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.491-3640_491-3639d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558162 | ||||||
| chr18:66558184
|
A | G | 2 | a0001c0003t0004g0169a0001c0003t0004g0197 | 2 | HG02080.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.491-3660T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558184 | ||||||
| chr18:66558280
|
C | T | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-3756G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558280 | ||||||
| chr18:66558308
|
G | A | 2 | a0001c0003t0004g0132a0001c0003t0004g0220 | 2 | NA18939.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.491-3784C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558308 | ||||||
| chr18:66558380
|
T | C | 1 | a0002c0004t0028g0178 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.491-3856A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558380 | ||||||
| chr18:66558387
|
T | C | 1 | a0001c0003t0004g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.491-3863A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558387 | ||||||
| chr18:66558434
|
C | A | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-3910G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558434 | ||||||
| chr18:66558722
|
T | A | 4 | a0001c0001t0009g0130a0001c0001t0009g0146a0001c0001t0009g0219others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-4198A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558722 | ||||||
| chr18:66558774
|
G | C | 1 | a0001c0001t0009g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.491-4250C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558774 | ||||||
| chr18:66558780
|
T | C | 7 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.491-4256A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558780 | ||||||
| chr18:66558881
|
T | G | 1 | a0001c0024t0002g0134 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.491-4357A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558881 | ||||||
| chr18:66558986
|
T | G | 1 | a0005c0009t0011g0248 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491-4462A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66558986 | ||||||
| chr18:66559011
|
G | T | 1 | a0001c0001t0006g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.491-4487C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559011 | ||||||
| chr18:66559032
|
G | A | 46 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(43): Show | 46 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.491-4508C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559032 | ||||||
| chr18:66559102
|
A | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.491-4578T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559102 | ||||||
| chr18:66559402
|
A | C | 1 | a0001c0001t0002g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.491-4878T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559402 | ||||||
| chr18:66559474
|
T | C | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.491-4950A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559474 | ||||||
| chr18:66559520
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.491-4996A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559520 | ||||||
| chr18:66559668
|
T | A | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.491-5144A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559668 | ||||||
| chr18:66559674
|
A | G | 1 | a0001c0001t0039g0319 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.491-5150T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559674 | ||||||
| chr18:66559677
|
A | AAT | 127 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.491-5155_491-5154d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559677 | ||||||
| chr18:66559740
|
A | G | 1 | a0001c0001t0002g0093 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.491-5216T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559740 | ||||||
| chr18:66559870
|
A | G | 80 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(77): Show | 81 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.491-5346T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559870 | ||||||
| chr18:66559900
|
A | G | 4 | a0004c0006t0004g0024a0004c0006t0004g0125a0004c0006t0004g0150others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-5376T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559900 | ||||||
| chr18:66559977
|
T | C | 2 | a0001c0003t0004g0171a0001c0003t0004g0184 | 2 | NA18955.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.491-5453A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66559977 | ||||||
| chr18:66560000
|
T | C | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-5476A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560000 | ||||||
| chr18:66560095
|
C | A | 8 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0002t0001g0201others(5): Show | 8 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-5571G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560095 | ||||||
| chr18:66560189
|
A | G | 1 | a0001c0010t0001g0308 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.491-5665T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560189 | ||||||
| chr18:66560239
|
G | T | 2 | a0001c0002t0001g0201a0001c0002t0001g0202 | 2 | NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.491-5715C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560239 | ||||||
| chr18:66560502
|
A | G | 2 | a0001c0001t0003g0338a0001c0001t0003g0339 | 2 | NA18999.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.491-5978T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560502 | ||||||
| chr18:66560538
|
A | T | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.491-6014T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560538 | ||||||
| chr18:66560781
|
T | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18991.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.491-6257A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560781 | ||||||
| chr18:66560959
|
A | G | 7 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.491-6435T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560959 | ||||||
| chr18:66560964
|
CT | C | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-6441delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560964 | ||||||
| chr18:66560966
|
T | A | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-6442A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66560966 | ||||||
| chr18:66561081
|
T | C | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-6557A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561081 | ||||||
| chr18:66561115
|
T | TA | 15 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0010g0012others(12): Show | 16 | HG01255.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.491-6592dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561115 | ||||||
| chr18:66561192
|
T | G | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-6668A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561192 | ||||||
| chr18:66561288
|
T | A | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.491-6764A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561288 | ||||||
| chr18:66561366
|
A | G | 1 | a0001c0001t0002g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.491-6842T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561366 | ||||||
| chr18:66561378
|
A | G | 1 | a0001c0001t0015g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.491-6854T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561378 | ||||||
| chr18:66561587
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.490+6829T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561587 | ||||||
| chr18:66561672
|
G | T | 1 | a0001c0003t0004g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.490+6744C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561672 | ||||||
| chr18:66561700
|
A | G | 1 | a0001c0001t0002g0351 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.490+6716T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66561700 | ||||||
| chr18:66562045
|
C | T | 4 | a0001c0001t0027g0180a0005c0009t0011g0025a0005c0009t0011g0247others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+6371G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562045 | ||||||
| chr18:66562280
|
T | TC | 3 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0243 | 3 | HG03710.hp1 NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.490+6135dupG | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562280 | ||||||
| chr18:66562293
|
T | G | 4 | a0001c0001t0027g0180a0005c0009t0011g0025a0005c0009t0011g0247others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+6123A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562293 | ||||||
| chr18:66562358
|
A | G | 1 | a0013c0016t0003g0042 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.490+6058T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562358 | ||||||
| chr18:66562611
|
C | A | 1 | a0001c0003t0014g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.490+5805G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562611 | ||||||
| chr18:66562648
|
C | T | 10 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(7): Show | 10 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+5768G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562648 | ||||||
| chr18:66562655
|
T | A | 1 | a0002c0004t0012g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.490+5761A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562655 | ||||||
| chr18:66562832
|
T | C | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490+5584A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562832 | ||||||
| chr18:66562883
|
A | G | 2 | a0001c0001t0003g0348a0001c0001t0032g0200 | 2 | NA19057.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.490+5533T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562883 | ||||||
| chr18:66562884
|
T | C | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+5532A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562884 | ||||||
| chr18:66562918
|
T | C | 3 | a0001c0001t0003g0324a0001c0001t0003g0338a0001c0001t0003g0339 | 3 | NA18999.hp2 NA19000.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.490+5498A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66562918 | ||||||
| chr18:66563044
|
T | C | 1 | a0001c0001t0013g0057 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.490+5372A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563044 | ||||||
| chr18:66563094
|
C | T | 5 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0002t0001g0201others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+5322G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563094 | ||||||
| chr18:66563117
|
A | G | 120 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.490+5299T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563117 | ||||||
| chr18:66563152
|
G | A | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.490+5264C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563152 | ||||||
| chr18:66563167
|
G | A | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490+5249C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563167 | ||||||
| chr18:66563456
|
G | A | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.490+4960C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563456 | ||||||
| chr18:66563597
|
G | C | 42 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0083others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.490+4819C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563597 | ||||||
| chr18:66563932
|
CTG | C | 26 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0004g0007others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.490+4482_490+4483d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563932 | ||||||
| chr18:66563957
|
T | C | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+4459A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66563957 | ||||||
| chr18:66564011
|
C | T | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.490+4405G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564011 | ||||||
| chr18:66564391
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.490+4025C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564391 | ||||||
| chr18:66564614
|
T | C | 6 | a0001c0001t0003g0058a0001c0001t0003g0067a0001c0001t0003g0070others(3): Show | 6 | HG01257.hp1 HG01934.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+3802A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564614 | ||||||
| chr18:66564720
|
G | A | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.490+3696C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564720 | ||||||
| chr18:66564766
|
G | C | 1 | a0001c0001t0003g0072 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.490+3650C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564766 | ||||||
| chr18:66564847
|
G | C | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(44): Show | 47 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.490+3569C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564847 | ||||||
| chr18:66564865
|
C | CT | 24 | a0001c0001t0003g0002a0001c0001t0003g0179a0001c0001t0003g0230others(21): Show | 25 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.490+3550dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564865 | ||||||
| chr18:66564865
|
CT | C | 157 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0078others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.490+3550delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564865 | ||||||
| chr18:66564865
|
CTT | C | 21 | a0001c0001t0002g0274a0001c0001t0003g0186a0001c0001t0017g0182others(18): Show | 21 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.490+3549_490+3550d others(4): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564865 | ||||||
| chr18:66564886
|
A | G | 1 | a0002c0004t0005g0285 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.490+3530T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564886 | ||||||
| chr18:66564946
|
C | G | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490+3470G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66564946 | ||||||
| chr18:66565093
|
A | T | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490+3323T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66565093 | ||||||
| chr18:66565132
|
T | A | 1 | a0012c0022t0008g0291 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.490+3284A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66565132 | ||||||
| chr18:66565150
|
A | C | 1 | a0001c0001t0010g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.490+3266T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66565150 | ||||||
| chr18:66565423
|
C | T | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490+2993G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66565423 | ||||||
| chr18:66565522
|
T | C | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.490+2894A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66565522 | ||||||
| chr18:66565614
|
G | A | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(44): Show | 47 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.490+2802C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66565614 | ||||||
| chr18:66565701
|
C | A | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.490+2715G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66565701 | ||||||
| chr18:66566051
|
A | C | 1 | a0001c0001t0002g0333 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.490+2365T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566051 | ||||||
| chr18:66566191
|
A | T | 1 | a0001c0001t0003g0300 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.490+2225T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566191 | ||||||
| chr18:66566280
|
C | CT | 15 | a0001c0001t0002g0102a0001c0001t0007g0268a0001c0001t0013g0022others(12): Show | 15 | HG01258.hp1 HG01358.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.490+2135dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566280 | ||||||
| chr18:66566280
|
CT | C | 12 | a0001c0001t0003g0067a0001c0001t0003g0121a0001c0001t0003g0324others(9): Show | 12 | HG01167.hp1 HG01257.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.490+2135delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566280 | ||||||
| chr18:66566424
|
A | G | 228 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.490+1992T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566424 | ||||||
| chr18:66566833
|
T | A | 2 | a0001c0001t0003g0249a0001c0001t0015g0246 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.490+1583A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566833 | ||||||
| chr18:66566845
|
G | A | 1 | a0001c0002t0001g0318 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.490+1571C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566845 | ||||||
| chr18:66566862
|
T | A | 1 | a0001c0001t0032g0200 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.490+1554A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566862 | ||||||
| chr18:66566870
|
A | G | 1 | a0001c0001t0011g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.490+1546T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566870 | ||||||
| chr18:66566873
|
G | A | 80 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(77): Show | 81 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.490+1543C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66566873 | ||||||
| chr18:66567111
|
A | T | 7 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.490+1305T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567111 | ||||||
| chr18:66567151
|
T | C | 1 | a0001c0001t0009g0118 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490+1265A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567151 | ||||||
| chr18:66567253
|
A | C | 2 | a0002c0004t0005g0119a0002c0004t0005g0298 | 2 | HG03239.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.490+1163T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567253 | ||||||
| chr18:66567363
|
G | A | 1 | a0001c0001t0007g0268 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.490+1053C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567363 | ||||||
| chr18:66567383
|
T | A | 1 | a0001c0003t0004g0181 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.490+1033A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567383 | ||||||
| chr18:66567460
|
T | C | 3 | a0006c0007t0006g0188a0006c0007t0014g0191a0006c0007t0029g0187 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.490+956A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567460 | ||||||
| chr18:66567600
|
T | C | 1 | a0001c0001t0024g0003 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.490+816A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567600 | ||||||
| chr18:66567978
|
A | C | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(44): Show | 47 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.490+438T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567978 | ||||||
| chr18:66567979
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.490+437C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567979 | ||||||
| chr18:66567983
|
T | C | 2 | a0001c0001t0003g0230a0001c0001t0003g0300 | 2 | NA18942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.490+433A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66567983 | ||||||
| chr18:66568079
|
T | C | 3 | a0005c0009t0011g0025a0005c0009t0011g0247a0005c0009t0011g0248 | 3 | HG02559.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.490+337A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66568079 | ||||||
| chr18:66568161
|
C | T | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.490+255G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66568161 | ||||||
| chr18:66568162
|
G | A | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.490+254C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66568162 | ||||||
| chr18:66568351
|
T | C | 1 | a0001c0001t0003g0350 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.490+65A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66568351 | ||||||
| chr18:66568388
|
A | G | 4 | a0004c0006t0004g0024a0004c0006t0004g0125a0004c0006t0004g0150others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+28T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 3/11 | chr18 | 66568388 | ||||||
| chr18:66568751
|
G | C | 1 | a0001c0002t0001g0330 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.196-41C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66568751 | ||||||
| chr18:66569327
|
A | G | 1 | a0001c0001t0011g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196-617T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66569327 | ||||||
| chr18:66569777
|
A | G | 13 | a0001c0001t0002g0026a0001c0001t0006g0073a0001c0001t0010g0012others(10): Show | 14 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-1067T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66569777 | ||||||
| chr18:66569896
|
A | T | 217 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.196-1186T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66569896 | ||||||
| chr18:66569972
|
T | C | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-1262A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66569972 | ||||||
| chr18:66570587
|
TACTA | T | 7 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+1419_195+1422d others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66570587 | ||||||
| chr18:66570632
|
T | A | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.195+1378A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66570632 | ||||||
| chr18:66570692
|
T | C | 1 | a0004c0006t0004g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.195+1318A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66570692 | ||||||
| chr18:66570799
|
A | G | 7 | a0001c0001t0002g0203a0001c0001t0003g0045a0001c0001t0003g0046others(4): Show | 7 | NA18965.hp1 NA18966.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+1211T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66570799 | ||||||
| chr18:66570985
|
G | A | 4 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+1025C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66570985 | ||||||
| chr18:66571021
|
C | T | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.195+989G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571021 | ||||||
| chr18:66571022
|
G | A | 2 | a0001c0001t0017g0182a0001c0001t0023g0190 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.195+988C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571022 | ||||||
| chr18:66571336
|
A | G | 78 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0053others(75): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+674T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571336 | ||||||
| chr18:66571407
|
T | C | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.195+603A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571407 | ||||||
| chr18:66571523
|
G | A | 4 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+487C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571523 | ||||||
| chr18:66571540
|
T | C | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+470A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571540 | ||||||
| chr18:66571887
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.195+123G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571887 | ||||||
| chr18:66571941
|
C | G | 1 | a0001c0001t0002g0352 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.195+69G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571941 | ||||||
| chr18:66571959
|
T | C | 20 | a0002c0004t0005g0017a0002c0004t0005g0119a0002c0004t0005g0128others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.195+51A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 2/11 | chr18 | 66571959 | ||||||
| chr18:66572668
|
A | G | 2 | a0004c0006t0004g0150a0004c0006t0014g0235 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-112-352T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66572668 | ||||||
| chr18:66572822
|
A | C | 1 | a0001c0003t0019g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-112-506T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66572822 | ||||||
| chr18:66572909
|
G | A | 2 | a0007c0012t0021g0090a0009c0019t0021g0310 | 2 | HG00140.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-112-593C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66572909 | ||||||
| chr18:66573316
|
A | C | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-112-1000T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573316 | ||||||
| chr18:66573362
|
G | A | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-1046C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573362 | ||||||
| chr18:66573615
|
T | C | 222 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-112-1299A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573615 | ||||||
| chr18:66573631
|
T | TA | 222 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-112-1316_-112-131 others(5): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573631 | ||||||
| chr18:66573633
|
T | G | 1 | a0001c0001t0020g0001 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-112-1317A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573633 | ||||||
| chr18:66573727
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-112-1411A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573727 | ||||||
| chr18:66573760
|
G | A | 2 | a0001c0001t0004g0075a0001c0001t0014g0076 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-112-1444C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573760 | ||||||
| chr18:66573859
|
C | T | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-1543G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573859 | ||||||
| chr18:66573893
|
C | CCA | 36 | a0001c0001t0002g0085a0001c0001t0003g0199a0001c0001t0003g0315others(33): Show | 36 | HG00642.hp2 HG01070.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.-112-1579_-112-157 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573893 | ||||||
| chr18:66573893
|
C | CCACA | 16 | a0001c0002t0001g0129a0001c0002t0001g0157a0001c0002t0001g0240others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.-112-1581_-112-157 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573893 | ||||||
| chr18:66573893
|
C | CCACACA | 94 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0186others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.-112-1583_-112-157 others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573893 | ||||||
| chr18:66573893
|
C | CCACACAC others(1): Show |
15 | a0001c0001t0003g0114a0001c0001t0003g0121a0001c0001t0003g0249others(12): Show | 15 | HG01934.hp1 HG01978.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-112-1585_-112-157 others(12): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573893 | ||||||
| chr18:66573893
|
C | CCACACAC others(3): Show |
7 | a0001c0002t0001g0023a0001c0002t0001g0065a0001c0002t0001g0071others(4): Show | 7 | HG01928.hp2 NA18942.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.-112-1587_-112-157 others(14): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573893 | ||||||
| chr18:66573893
|
C | CCACACAC others(5): Show |
1 | a0001c0002t0001g0066 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-112-1589_-112-157 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573893 | ||||||
| chr18:66573893
|
CCA | C | 18 | a0001c0001t0002g0026a0001c0001t0002g0207a0001c0001t0002g0274others(15): Show | 19 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-112-1579_-112-157 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573893 | ||||||
| chr18:66573893
|
CCACA | C | 7 | a0001c0001t0002g0087a0001c0001t0011g0014a0001c0001t0011g0099others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112-1581_-112-157 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573893 | ||||||
| chr18:66573919
|
ACAC | A | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-1606_-112-160 others(7): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66573919 | ||||||
| chr18:66574153
|
C | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0142a0001c0002t0001g0320others(1): Show | 4 | HG00733.hp2 HG01169.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-1837G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574153 | ||||||
| chr18:66574244
|
AT | A | 4 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-1929delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574244 | ||||||
| chr18:66574383
|
A | G | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(44): Show | 47 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-112-2067T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574383 | ||||||
| chr18:66574677
|
C | T | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-2361G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574677 | ||||||
| chr18:66574707
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-112-2391A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574707 | ||||||
| chr18:66574729
|
G | A | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-112-2413C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574729 | ||||||
| chr18:66574760
|
A | C | 4 | a0002c0004t0005g0275a0002c0004t0005g0276a0002c0004t0005g0278others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-2444T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574760 | ||||||
| chr18:66574912
|
A | T | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-112-2596T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574912 | ||||||
| chr18:66574954
|
G | T | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-112-2638C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66574954 | ||||||
| chr18:66575041
|
C | A | 27 | a0001c0001t0002g0026a0001c0001t0002g0274a0001c0001t0006g0073others(24): Show | 28 | HG01109.hp1 HG01255.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.-112-2725G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66575041 | ||||||
| chr18:66575225
|
C | CGGGGGAG others(4): Show |
1 | a0001c0003t0004g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-112-2920_-112-291 others(15): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66575225 | ||||||
| chr18:66575226
|
G | A | 8 | a0001c0001t0002g0147a0001c0001t0002g0205a0001c0001t0002g0207others(5): Show | 8 | HG00544.hp1 HG02083.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112-2910C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66575226 | ||||||
| chr18:66575374
|
A | G | 1 | a0001c0001t0003g0300 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-112-3058T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66575374 | ||||||
| chr18:66575755
|
C | T | 4 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-3439G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66575755 | ||||||
| chr18:66575808
|
C | A | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-112-3492G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66575808 | ||||||
| chr18:66575941
|
T | C | 1 | a0001c0002t0001g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-112-3625A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66575941 | ||||||
| chr18:66575964
|
T | C | 2 | a0001c0003t0004g0132a0001c0003t0004g0220 | 2 | NA18939.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-112-3648A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66575964 | ||||||
| chr18:66576083
|
A | C | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-112-3767T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66576083 | ||||||
| chr18:66576208
|
T | C | 3 | a0001c0010t0001g0280a0001c0010t0001g0308a0001c0011t0002g0306 | 3 | HG00323.hp1 HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-112-3892A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66576208 | ||||||
| chr18:66576395
|
G | T | 2 | a0001c0001t0017g0182a0001c0001t0023g0190 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-112-4079C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66576395 | ||||||
| chr18:66576622
|
A | T | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-112-4306T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66576622 | ||||||
| chr18:66576883
|
G | C | 2 | a0006c0007t0006g0188a0006c0007t0029g0187 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-112-4567C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66576883 | ||||||
| chr18:66576981
|
A | T | 1 | a0001c0001t0017g0137 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-112-4665T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66576981 | ||||||
| chr18:66577132
|
T | C | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-112-4816A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577132 | ||||||
| chr18:66577147
|
T | C | 8 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(5): Show | 8 | HG01255.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112-4831A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577147 | ||||||
| chr18:66577260
|
A | T | 1 | a0001c0001t0002g0215 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-112-4944T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577260 | ||||||
| chr18:66577268
|
G | T | 2 | a0001c0003t0019g0027a0001c0003t0019g0028 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-112-4952C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577268 | ||||||
| chr18:66577467
|
A | G | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-112-5151T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577467 | ||||||
| chr18:66577509
|
A | G | 5 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0002t0001g0201others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-5193T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577509 | ||||||
| chr18:66577520
|
A | C | 1 | a0001c0001t0002g0335 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-112-5204T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577520 | ||||||
| chr18:66577547
|
C | T | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-112-5231G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577547 | ||||||
| chr18:66577584
|
T | C | 1 | a0001c0001t0004g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-112-5268A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577584 | ||||||
| chr18:66577656
|
A | T | 2 | a0001c0002t0001g0156a0001c0002t0001g0166 | 2 | HG02056.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-112-5340T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66577656 | ||||||
| chr18:66578165
|
C | T | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-5849G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66578165 | ||||||
| chr18:66578312
|
C | T | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-112-5996G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66578312 | ||||||
| chr18:66578373
|
T | A | 1 | a0001c0003t0004g0267 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-112-6057A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66578373 | ||||||
| chr18:66578395
|
C | T | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-112-6079G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66578395 | ||||||
| chr18:66578481
|
C | T | 310 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(307): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-112-6165G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66578481 | ||||||
| chr18:66578821
|
A | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-112-6505T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66578821 | ||||||
| chr18:66578912
|
A | C | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-112-6596T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66578912 | ||||||
| chr18:66578958
|
C | T | 1 | a0001c0001t0017g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-112-6642G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66578958 | ||||||
| chr18:66579084
|
A | G | 3 | a0005c0009t0011g0025a0005c0009t0011g0247a0005c0009t0011g0248 | 3 | HG02559.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-112-6768T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579084 | ||||||
| chr18:66579159
|
G | A | 3 | a0005c0009t0011g0025a0005c0009t0011g0247a0005c0009t0011g0248 | 3 | HG02559.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-112-6843C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579159 | ||||||
| chr18:66579271
|
T | TG | 4 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(1): Show | 4 | NA18947.hp2 NA18960.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-6956dupC | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579271 | ||||||
| chr18:66579376
|
G | A | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-112-7060C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579376 | ||||||
| chr18:66579426
|
C | T | 1 | a0001c0001t0003g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-112-7110G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579426 | ||||||
| chr18:66579473
|
G | A | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-7157C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579473 | ||||||
| chr18:66579499
|
C | T | 1 | a0001c0001t0011g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-112-7183G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579499 | ||||||
| chr18:66579558
|
A | T | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-7242T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579558 | ||||||
| chr18:66579580
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-112-7264T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579580 | ||||||
| chr18:66579585
|
G | T | 2 | a0001c0001t0002g0206a0001c0001t0002g0335 | 2 | HG00609.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-112-7269C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579585 | ||||||
| chr18:66579603
|
T | G | 1 | a0001c0003t0004g0181 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-112-7287A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579603 | ||||||
| chr18:66579705
|
C | T | 1 | a0001c0001t0010g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-112-7389G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579705 | ||||||
| chr18:66579825
|
G | C | 4 | a0001c0001t0011g0014a0001c0001t0011g0099a0001c0001t0011g0236others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-7509C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579825 | ||||||
| chr18:66579858
|
A | G | 6 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-7542T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579858 | ||||||
| chr18:66579871
|
C | T | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-7555G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579871 | ||||||
| chr18:66579877
|
T | A | 1 | a0012c0022t0008g0291 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-112-7561A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579877 | ||||||
| chr18:66579950
|
T | C | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-112-7634A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66579950 | ||||||
| chr18:66580017
|
C | T | 6 | a0003c0005t0022g0227a0003c0005t0022g0346a0003c0005t0026g0010others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-7701G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580017 | ||||||
| chr18:66580041
|
G | A | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-112-7725C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580041 | ||||||
| chr18:66580075
|
G | A | 27 | a0001c0001t0002g0026a0001c0001t0002g0274a0001c0001t0006g0073others(24): Show | 28 | HG01109.hp1 HG01255.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.-112-7759C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580075 | ||||||
| chr18:66580100
|
C | A | 4 | a0001c0001t0027g0180a0005c0009t0011g0025a0005c0009t0011g0247others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-7784G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580100 | ||||||
| chr18:66580398
|
T | G | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-112-8082A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580398 | ||||||
| chr18:66580406
|
T | G | 1 | a0001c0002t0001g0234 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-112-8090A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580406 | ||||||
| chr18:66580586
|
C | T | 2 | a0001c0002t0001g0156a0001c0002t0001g0166 | 2 | HG02056.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-112-8270G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580586 | ||||||
| chr18:66580783
|
A | C | 2 | a0001c0001t0002g0147a0001c0001t0002g0205 | 2 | HG00544.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.-112-8467T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580783 | ||||||
| chr18:66580838
|
A | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-112-8522T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580838 | ||||||
| chr18:66580909
|
C | A | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-112-8593G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580909 | ||||||
| chr18:66580914
|
C | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-112-8598G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66580914 | ||||||
| chr18:66581083
|
G | T | 4 | a0001c0001t0016g0086a0001c0001t0016g0327a0001c0001t0016g0342others(1): Show | 4 | HG00673.hp2 NA18956.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-8767C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581083 | ||||||
| chr18:66581118
|
G | A | 1 | a0002c0004t0012g0282 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-112-8802C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581118 | ||||||
| chr18:66581125
|
T | C | 1 | a0001c0001t0027g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-112-8809A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581125 | ||||||
| chr18:66581211
|
AG | A | 39 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0083others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-112-8896delC | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581211 | ||||||
| chr18:66581381
|
G | A | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-112-9065C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581381 | ||||||
| chr18:66581578
|
G | C | 1 | a0001c0001t0037g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-112-9262C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581578 | ||||||
| chr18:66581653
|
C | T | 1 | a0001c0011t0002g0306 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-112-9337G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581653 | ||||||
| chr18:66581755
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-112-9439G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581755 | ||||||
| chr18:66581792
|
C | T | 3 | a0005c0009t0011g0025a0005c0009t0011g0247a0005c0009t0011g0248 | 3 | HG02559.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-112-9476G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581792 | ||||||
| chr18:66581881
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-112-9565G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581881 | ||||||
| chr18:66581947
|
A | G | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0093others(44): Show | 47 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-112-9631T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66581947 | ||||||
| chr18:66582026
|
T | C | 1 | a0001c0001t0003g0230 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-112-9710A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582026 | ||||||
| chr18:66582127
|
T | C | 1 | a0001c0001t0003g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-112-9811A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582127 | ||||||
| chr18:66582135
|
A | T | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-112-9819T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582135 | ||||||
| chr18:66582551
|
T | A | 4 | a0001c0001t0003g0324a0001c0001t0003g0338a0001c0001t0003g0339others(1): Show | 4 | NA18998.hp1 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-10235A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582551 | ||||||
| chr18:66582639
|
C | CA | 145 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0034others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-112-10324dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582639 | ||||||
| chr18:66582639
|
C | CAA | 61 | a0001c0001t0002g0089a0001c0001t0002g0133a0001c0001t0002g0136others(58): Show | 61 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-112-10325_-112-10 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582639 | ||||||
| chr18:66582639
|
C | CAAA | 6 | a0001c0001t0002g0274a0001c0001t0015g0237a0001c0002t0001g0234others(3): Show | 6 | HG02886.hp1 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-10326_-112-10 others(9): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582639 | ||||||
| chr18:66582639
|
CA | C | 15 | a0001c0001t0003g0199a0001c0001t0004g0021a0001c0001t0004g0075others(12): Show | 15 | HG01074.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-112-10324delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582639 | ||||||
| chr18:66582893
|
C | T | 5 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0002t0001g0201others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-10577G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582893 | ||||||
| chr18:66582986
|
A | G | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112-10670T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66582986 | ||||||
| chr18:66583042
|
T | G | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-112-10726A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66583042 | ||||||
| chr18:66583049
|
G | A | 1 | a0001c0001t0011g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-112-10733C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66583049 | ||||||
| chr18:66583082
|
T | C | 1 | a0006c0007t0014g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-112-10766A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66583082 | ||||||
| chr18:66583107
|
G | A | 1 | a0001c0001t0020g0001 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-112-10791C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66583107 | ||||||
| chr18:66583478
|
C | T | 3 | a0005c0009t0011g0025a0005c0009t0011g0247a0005c0009t0011g0248 | 3 | HG02559.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-112-11162G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66583478 | ||||||
| chr18:66583600
|
G | T | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-112-11284C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66583600 | ||||||
| chr18:66583849
|
A | T | 4 | a0001c0001t0023g0190a0006c0007t0006g0188a0006c0007t0014g0191others(1): Show | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-11533T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66583849 | ||||||
| chr18:66583857
|
T | C | 2 | a0007c0012t0021g0090a0009c0019t0021g0310 | 2 | HG00140.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-112-11541A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66583857 | ||||||
| chr18:66584039
|
A | T | 1 | a0001c0001t0007g0177 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-112-11723T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584039 | ||||||
| chr18:66584068
|
C | T | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-112-11752G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584068 | ||||||
| chr18:66584071
|
C | A | 2 | a0001c0001t0003g0249a0001c0001t0015g0246 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-112-11755G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584071 | ||||||
| chr18:66584103
|
T | A | 2 | a0001c0002t0001g0201a0001c0002t0001g0202 | 2 | NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-112-11787A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584103 | ||||||
| chr18:66584238
|
C | A | 128 | a0001c0001t0002g0034a0001c0001t0002g0256a0001c0001t0003g0114others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-112-11922G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584238 | ||||||
| chr18:66584289
|
G | T | 1 | a0001c0001t0039g0319 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-112-11973C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584289 | ||||||
| chr18:66584321
|
T | C | 219 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-112-12005A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584321 | ||||||
| chr18:66584321
|
T | G | 7 | a0001c0001t0002g0274a0001c0001t0017g0182a0001c0001t0023g0190others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112-12005A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584321 | ||||||
| chr18:66584353
|
A | G | 228 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0026others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.-112-12037T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584353 | ||||||
| chr18:66584383
|
T | C | 2 | a0001c0001t0017g0182a0001c0001t0023g0190 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-112-12067A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584383 | ||||||
| chr18:66584580
|
A | T | 4 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(1): Show | 4 | HG00609.hp2 HG02129.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-12264T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584580 | ||||||
| chr18:66584870
|
C | T | 1 | a0001c0001t0015g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-112-12554G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584870 | ||||||
| chr18:66584923
|
T | G | 1 | a0006c0007t0014g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-112-12607A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584923 | ||||||
| chr18:66584968
|
T | G | 1 | a0001c0002t0001g0060 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-112-12652A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584968 | ||||||
| chr18:66584969
|
G | A | 2 | a0001c0001t0003g0123a0001c0001t0038g0124 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-112-12653C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66584969 | ||||||
| chr18:66585104
|
T | C | 40 | a0001c0001t0003g0011a0001c0001t0003g0179a0001c0001t0003g0193others(37): Show | 40 | HG00639.hp2 HG00673.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.-112-12788A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585104 | ||||||
| chr18:66585252
|
T | C | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-112-12936A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585252 | ||||||
| chr18:66585318
|
C | T | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0034others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-112-13002G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585318 | ||||||
| chr18:66585564
|
T | C | 42 | a0001c0001t0002g0091a0001c0001t0002g0168a0001c0001t0003g0114others(39): Show | 42 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-112-13248A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585564 | ||||||
| chr18:66585574
|
G | A | 2 | a0001c0001t0013g0217a0001c0001t0013g0225 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-112-13258C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585574 | ||||||
| chr18:66585590
|
G | A | 3 | a0001c0001t0010g0139a0001c0001t0010g0250a0001c0001t0010g0251 | 3 | HG02723.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-112-13274C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585590 | ||||||
| chr18:66585644
|
G | C | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-13328C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585644 | ||||||
| chr18:66585929
|
T | C | 5 | a0001c0001t0017g0018a0001c0002t0001g0030a0001c0003t0019g0027others(2): Show | 5 | HG02896.hp2 HG03225.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112-13613A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585929 | ||||||
| chr18:66585933
|
A | G | 5 | a0001c0001t0007g0177a0001c0002t0001g0173a0001c0002t0001g0174others(2): Show | 5 | HG00609.hp2 HG02129.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112-13617T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585933 | ||||||
| chr18:66585954
|
C | T | 1 | a0001c0001t0010g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-112-13638G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585954 | ||||||
| chr18:66585974
|
A | G | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-112-13658T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66585974 | ||||||
| chr18:66586016
|
T | C | 1 | a0001c0001t0003g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-112-13700A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586016 | ||||||
| chr18:66586031
|
C | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-112-13715G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586031 | ||||||
| chr18:66586180
|
A | G | 1 | a0001c0001t0017g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-112-13864T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586180 | ||||||
| chr18:66586196
|
T | A | 3 | a0001c0001t0003g0121a0001c0002t0001g0120a0002c0004t0005g0119 | 3 | HG02738.hp1 HG02976.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-112-13880A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586196 | ||||||
| chr18:66586208
|
G | A | 3 | a0001c0003t0019g0027a0001c0003t0019g0028a0001c0003t0019g0029 | 3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-112-13892C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586208 | ||||||
| chr18:66586429
|
G | A | 3 | a0001c0003t0004g0171a0001c0003t0004g0184a0001c0003t0041g0170 | 3 | NA18955.hp2 NA18999.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-112-14113C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586429 | ||||||
| chr18:66586564
|
A | C | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-112-14248T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586564 | ||||||
| chr18:66586587
|
T | C | 4 | a0001c0001t0006g0100a0001c0001t0006g0110a0001c0001t0006g0111others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-14271A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586587 | ||||||
| chr18:66586607
|
A | T | 1 | a0001c0001t0004g0007 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-112-14291T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586607 | ||||||
| chr18:66586640
|
G | C | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-112-14324C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586640 | ||||||
| chr18:66586654
|
G | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-112-14338C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586654 | ||||||
| chr18:66586807
|
G | C | 1 | a0001c0001t0035g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-112-14491C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586807 | ||||||
| chr18:66586844
|
G | A | 5 | a0001c0001t0007g0177a0001c0002t0001g0173a0001c0002t0001g0174others(2): Show | 5 | HG00609.hp2 HG02129.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112-14528C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586844 | ||||||
| chr18:66586927
|
C | T | 4 | a0001c0001t0003g0123a0001c0001t0038g0124a0001c0002t0001g0122others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-14611G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586927 | ||||||
| chr18:66586959
|
T | C | 1 | a0001c0001t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-112-14643A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66586959 | ||||||
| chr18:66587051
|
C | T | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112-14735G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587051 | ||||||
| chr18:66587090
|
T | C | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112-14774A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587090 | ||||||
| chr18:66587127
|
G | C | 2 | a0003c0005t0022g0227a0003c0005t0043g0228 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-112-14811C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587127 | ||||||
| chr18:66587268
|
C | T | 1 | a0010c0020t0036g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-112-14952G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587268 | ||||||
| chr18:66587274
|
G | A | 1 | a0001c0002t0001g0323 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-112-14958C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587274 | ||||||
| chr18:66587388
|
A | C | 1 | a0001c0002t0008g0127 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-112-15072T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587388 | ||||||
| chr18:66587394
|
A | G | 2 | a0003c0005t0022g0227a0003c0005t0043g0228 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-112-15078T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587394 | ||||||
| chr18:66587436
|
A | C | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-112-15120T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587436 | ||||||
| chr18:66587472
|
G | A | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-112-15156C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587472 | ||||||
| chr18:66587472
|
G | T | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-112-15156C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587472 | ||||||
| chr18:66587574
|
C | A | 4 | a0001c0001t0003g0123a0001c0001t0038g0124a0001c0002t0001g0122others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-15258G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587574 | ||||||
| chr18:66587626
|
G | A | 26 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0083others(23): Show | 26 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.-112-15310C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587626 | ||||||
| chr18:66587685
|
G | A | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-112-15369C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587685 | ||||||
| chr18:66587765
|
C | T | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112-15449G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587765 | ||||||
| chr18:66587862
|
C | A | 1 | a0001c0001t0020g0001 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-112-15546G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66587862 | ||||||
| chr18:66588161
|
C | G | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+15793G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588161 | ||||||
| chr18:66588162
|
G | A | 3 | a0001c0001t0004g0007a0002c0004t0005g0119a0010c0020t0036g0009 | 3 | HG01934.hp1 HG02965.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-113+15792C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588162 | ||||||
| chr18:66588183
|
C | T | 199 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-113+15771G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588183 | ||||||
| chr18:66588389
|
T | A | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+15565A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588389 | ||||||
| chr18:66588429
|
G | A | 3 | a0001c0001t0011g0236a0001c0001t0015g0237a0004c0006t0014g0235 | 3 | HG01109.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-113+15525C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588429 | ||||||
| chr18:66588605
|
C | CATATATA others(3): Show |
5 | a0001c0001t0003g0339a0001c0001t0006g0255a0001c0008t0003g0303others(2): Show | 5 | HG00323.hp2 HG01433.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+15348_-113+15 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(5): Show |
7 | a0001c0001t0002g0274a0001c0001t0002g0287a0001c0001t0002g0335others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.-113+15348_-113+15 others(18): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(11): Show |
1 | a0001c0011t0002g0306 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-113+15348_-113+15 others(24): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(7): Show |
19 | a0001c0001t0002g0301a0001c0001t0002g0309a0001c0001t0002g0333others(16): Show | 19 | HG00438.hp1 HG00738.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-113+15348_-113+15 others(20): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(9): Show |
27 | a0001c0001t0003g0265a0001c0001t0003g0270a0001c0001t0003g0271others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.-113+15348_-113+15 others(22): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(11): Show |
15 | a0001c0001t0002g0288a0001c0001t0002g0312a0001c0001t0003g0290others(12): Show | 15 | HG00642.hp1 HG01109.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-113+15348_-113+15 others(24): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(13): Show |
6 | a0001c0001t0002g0254a0001c0001t0003g0313a0001c0001t0003g0315others(3): Show | 6 | HG00735.hp2 HG01496.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113+15348_-113+15 others(26): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(15): Show |
3 | a0001c0001t0003g0345a0001c0001t0016g0327a0001c0002t0018g0340 | 3 | HG00140.hp1 NA18949.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-113+15348_-113+15 others(28): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(17): Show |
6 | a0001c0001t0004g0344a0001c0001t0016g0342a0001c0002t0001g0273others(3): Show | 6 | HG00558.hp1 HG00741.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113+15348_-113+15 others(30): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588605
|
C | CATATATA others(19): Show |
1 | a0001c0001t0002g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-113+15348_-113+15 others(32): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588605 | ||||||
| chr18:66588614
|
C | A | 94 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0287others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.-113+15340G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588614 | ||||||
| chr18:66588620
|
C | A | 97 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0287others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.-113+15334G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588620 | ||||||
| chr18:66588620
|
C | CTA | 7 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+15332_-113+15 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588620 | ||||||
| chr18:66588626
|
C | A | 106 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-113+15328G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588626 | ||||||
| chr18:66588626
|
C | CTA | 3 | a0001c0001t0003g0121a0001c0002t0001g0120a0002c0004t0005g0119 | 3 | HG02738.hp1 HG02976.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-113+15326_-113+15 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588626 | ||||||
| chr18:66588632
|
A | C | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+15322T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588632 | ||||||
| chr18:66588635
|
T | G | 8 | a0001c0001t0003g0011a0001c0001t0006g0013a0001c0001t0010g0012others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-113+15319A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588635 | ||||||
| chr18:66588639
|
G | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+15315C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588639 | ||||||
| chr18:66588695
|
A | G | 1 | a0001c0001t0032g0200 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-113+15259T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588695 | ||||||
| chr18:66588818
|
A | C | 1 | a0003c0005t0022g0346 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-113+15136T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588818 | ||||||
| chr18:66588854
|
C | T | 1 | a0001c0001t0006g0255 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-113+15100G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66588854 | ||||||
| chr18:66589188
|
C | A | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+14766G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589188 | ||||||
| chr18:66589201
|
G | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+14753C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589201 | ||||||
| chr18:66589233
|
C | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+14721G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589233 | ||||||
| chr18:66589251
|
C | CAT | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+14701_-113+14 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589251 | ||||||
| chr18:66589263
|
T | C | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113+14691A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589263 | ||||||
| chr18:66589266
|
A | C | 2 | a0001c0001t0004g0075a0001c0001t0014g0076 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-113+14688T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589266 | ||||||
| chr18:66589269
|
C | T | 2 | a0001c0001t0013g0217a0001c0001t0013g0225 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-113+14685G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589269 | ||||||
| chr18:66589271
|
T | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(19): Show | 22 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.-113+14683A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589271 | ||||||
| chr18:66589344
|
C | T | 1 | a0001c0001t0010g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-113+14610G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589344 | ||||||
| chr18:66589393
|
A | T | 156 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-113+14561T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589393 | ||||||
| chr18:66589401
|
T | A | 2 | a0001c0001t0010g0012a0001c0001t0010g0016 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-113+14553A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589401 | ||||||
| chr18:66589473
|
T | C | 13 | a0001c0001t0002g0203a0001c0001t0002g0205a0001c0001t0002g0206others(10): Show | 13 | HG00609.hp1 HG02083.hp2 HG03492.hp2 others(10): Show |
intron_variant | MODIFIER | c.-113+14481A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589473 | ||||||
| chr18:66589519
|
G | C | 1 | a0001c0001t0015g0237 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-113+14435C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589519 | ||||||
| chr18:66589533
|
C | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-113+14421G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589533 | ||||||
| chr18:66589576
|
T | A | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+14378A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589576 | ||||||
| chr18:66589595
|
T | C | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113+14359A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589595 | ||||||
| chr18:66589598
|
A | T | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113+14356T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589598 | ||||||
| chr18:66589599
|
TAAATTTA others(102): Show |
T | 1 | a0003c0005t0034g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113+14246_-113+14 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589599 | ||||||
| chr18:66589610
|
T | A | 1 | a0001c0001t0009g0118 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-113+14344A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589610 | ||||||
| chr18:66589663
|
C | T | 191 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-113+14291G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589663 | ||||||
| chr18:66589675
|
G | A | 1 | a0001c0010t0001g0280 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-113+14279C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589675 | ||||||
| chr18:66589707
|
A | AAC | 191 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-113+14245_-113+14 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589707 | ||||||
| chr18:66589720
|
G | A | 3 | a0001c0001t0003g0179a0001c0003t0004g0185a0002c0004t0028g0178 | 3 | HG00639.hp2 HG00642.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-113+14234C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589720 | ||||||
| chr18:66589833
|
T | C | 1 | a0001c0001t0011g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-113+14121A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589833 | ||||||
| chr18:66589937
|
G | A | 1 | a0001c0001t0007g0092 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-113+14017C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589937 | ||||||
| chr18:66589976
|
T | TTTTA | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+13977_-113+13 others(10): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66589976 | ||||||
| chr18:66590128
|
G | T | 1 | a0001c0001t0004g0233 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-113+13826C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590128 | ||||||
| chr18:66590130
|
T | C | 8 | a0001c0001t0003g0186a0001c0001t0009g0192a0001c0001t0023g0190others(5): Show | 8 | HG00735.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-113+13824A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590130 | ||||||
| chr18:66590170
|
T | C | 3 | a0001c0001t0011g0236a0001c0001t0015g0237a0004c0006t0014g0235 | 3 | HG01109.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-113+13784A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590170 | ||||||
| chr18:66590184
|
T | C | 1 | a0001c0001t0003g0336 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-113+13770A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590184 | ||||||
| chr18:66590213
|
G | A | 1 | a0001c0001t0009g0322 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-113+13741C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590213 | ||||||
| chr18:66590350
|
C | G | 2 | a0002c0004t0005g0275a0002c0004t0005g0276 | 2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-113+13604G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590350 | ||||||
| chr18:66590379
|
T | G | 1 | a0001c0002t0025g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-113+13575A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590379 | ||||||
| chr18:66590395
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-113+13559C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590395 | ||||||
| chr18:66590450
|
G | T | 2 | a0001c0001t0003g0249a0001c0001t0015g0246 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-113+13504C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590450 | ||||||
| chr18:66590526
|
TA | T | 104 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.-113+13427delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590526 | ||||||
| chr18:66590526
|
TAA | T | 97 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(94): Show | 98 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+13426_-113+13 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590526 | ||||||
| chr18:66590552
|
A | G | 1 | a0015c0015t0004g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-113+13402T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590552 | ||||||
| chr18:66590561
|
T | C | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113+13393A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590561 | ||||||
| chr18:66590631
|
G | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+13323C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590631 | ||||||
| chr18:66590710
|
T | A | 1 | a0001c0001t0002g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-113+13244A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590710 | ||||||
| chr18:66590871
|
G | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+13083C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590871 | ||||||
| chr18:66590951
|
A | G | 2 | a0001c0001t0002g0274a0003c0005t0022g0346 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-113+13003T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66590951 | ||||||
| chr18:66591028
|
C | A | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113+12926G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591028 | ||||||
| chr18:66591076
|
C | G | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+12878G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591076 | ||||||
| chr18:66591124
|
T | A | 1 | a0001c0001t0010g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-113+12830A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591124 | ||||||
| chr18:66591251
|
C | A | 2 | a0001c0002t0001g0244a0002c0004t0012g0245 | 2 | HG01070.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-113+12703G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591251 | ||||||
| chr18:66591273
|
A | G | 3 | a0001c0002t0001g0138a0001c0002t0001g0223a0001c0002t0008g0127 | 3 | NA18968.hp1 NA18998.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-113+12681T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591273 | ||||||
| chr18:66591326
|
A | G | 1 | a0001c0001t0003g0035 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-113+12628T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591326 | ||||||
| chr18:66591535
|
G | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+12419C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591535 | ||||||
| chr18:66591546
|
A | G | 1 | a0001c0001t0003g0193 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-113+12408T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591546 | ||||||
| chr18:66591597
|
T | C | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+12357A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591597 | ||||||
| chr18:66591651
|
C | T | 2 | a0003c0005t0022g0227a0003c0005t0043g0228 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-113+12303G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591651 | ||||||
| chr18:66591661
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-113+12293A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591661 | ||||||
| chr18:66591709
|
A | G | 92 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0287others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.-113+12245T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591709 | ||||||
| chr18:66591748
|
T | C | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+12206A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591748 | ||||||
| chr18:66591853
|
C | T | 1 | a0001c0001t0006g0100 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-113+12101G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591853 | ||||||
| chr18:66591878
|
C | G | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+12076G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591878 | ||||||
| chr18:66591902
|
T | C | 1 | a0001c0001t0003g0114 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-113+12052A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66591902 | ||||||
| chr18:66592002
|
C | T | 4 | a0001c0001t0002g0034a0001c0001t0011g0236a0001c0001t0015g0237others(1): Show | 4 | HG01109.hp1 HG01891.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+11952G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592002 | ||||||
| chr18:66592252
|
T | C | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+11702A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592252 | ||||||
| chr18:66592464
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-113+11490A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592464 | ||||||
| chr18:66592474
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-113+11480C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592474 | ||||||
| chr18:66592501
|
C | T | 201 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-113+11453G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592501 | ||||||
| chr18:66592544
|
A | AT | 3 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0002t0001g0094 | 3 | HG00738.hp2 HG01346.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-113+11409dupA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592544 | ||||||
| chr18:66592620
|
C | G | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+11334G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592620 | ||||||
| chr18:66592657
|
C | T | 2 | a0001c0001t0017g0137a0002c0004t0012g0282 | 2 | HG01496.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-113+11297G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592657 | ||||||
| chr18:66592704
|
G | A | 1 | a0001c0001t0010g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-113+11250C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592704 | ||||||
| chr18:66592797
|
C | T | 7 | a0001c0001t0003g0121a0001c0001t0009g0116a0001c0001t0009g0117others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+11157G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592797 | ||||||
| chr18:66592937
|
T | C | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+11017A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66592937 | ||||||
| chr18:66593073
|
G | A | 1 | a0001c0002t0018g0257 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-113+10881C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593073 | ||||||
| chr18:66593075
|
C | T | 11 | a0001c0001t0002g0289a0001c0001t0002g0321a0001c0001t0003g0290others(8): Show | 11 | HG00733.hp2 HG01261.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-113+10879G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593075 | ||||||
| chr18:66593242
|
A | G | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113+10712T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593242 | ||||||
| chr18:66593350
|
T | C | 2 | a0001c0001t0002g0274a0003c0005t0022g0346 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-113+10604A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593350 | ||||||
| chr18:66593497
|
T | C | 2 | a0003c0005t0022g0227a0003c0005t0043g0228 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-113+10457A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593497 | ||||||
| chr18:66593505
|
G | T | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+10449C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593505 | ||||||
| chr18:66593542
|
C | A | 1 | a0001c0001t0002g0337 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-113+10412G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593542 | ||||||
| chr18:66593551
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-113+10403A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593551 | ||||||
| chr18:66593578
|
T | A | 3 | a0001c0001t0003g0324a0001c0001t0003g0338a0001c0001t0003g0339 | 3 | NA18999.hp2 NA19000.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-113+10376A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593578 | ||||||
| chr18:66593594
|
C | A | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+10360G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593594 | ||||||
| chr18:66593616
|
A | T | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113+10338T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593616 | ||||||
| chr18:66593649
|
G | C | 1 | a0001c0002t0001g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-113+10305C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593649 | ||||||
| chr18:66593701
|
A | G | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0083others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-113+10253T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593701 | ||||||
| chr18:66593987
|
CCACTTTT others(26): Show |
C | 1 | a0001c0001t0010g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-113+9934_-113+996 others(37): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66593987 | ||||||
| chr18:66594035
|
A | G | 1 | a0001c0001t0007g0266 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-113+9919T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594035 | ||||||
| chr18:66594071
|
T | A | 4 | a0001c0001t0003g0123a0001c0001t0038g0124a0001c0002t0001g0122others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+9883A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594071 | ||||||
| chr18:66594282
|
C | T | 4 | a0001c0001t0003g0123a0001c0001t0038g0124a0001c0002t0001g0122others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+9672G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594282 | ||||||
| chr18:66594379
|
A | T | 3 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0014g0076 | 3 | HG01074.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-113+9575T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594379 | ||||||
| chr18:66594410
|
T | C | 22 | a0001c0001t0002g0203a0001c0001t0002g0205a0001c0001t0002g0206others(19): Show | 22 | HG00609.hp1 HG02056.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.-113+9544A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594410 | ||||||
| chr18:66594534
|
G | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+9420C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594534 | ||||||
| chr18:66594556
|
C | T | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-113+9398G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594556 | ||||||
| chr18:66594577
|
A | G | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+9377T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594577 | ||||||
| chr18:66594602
|
A | ACCCCCCC others(26): Show |
1 | a0001c0001t0010g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-113+9351_-113+935 others(37): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594602 | ||||||
| chr18:66594675
|
A | G | 7 | a0001c0001t0003g0121a0001c0001t0009g0116a0001c0001t0009g0117others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+9279T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594675 | ||||||
| chr18:66594684
|
T | G | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+9270A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594684 | ||||||
| chr18:66594776
|
A | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-113+9178T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594776 | ||||||
| chr18:66594860
|
T | A | 1 | a0001c0001t0010g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-113+9094A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594860 | ||||||
| chr18:66594911
|
C | T | 10 | a0001c0001t0003g0011a0001c0001t0006g0013a0001c0001t0010g0012others(7): Show | 10 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-113+9043G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66594911 | ||||||
| chr18:66595026
|
T | TA | 96 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.-113+8927dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595026 | ||||||
| chr18:66595191
|
A | AAGCAGTG others(23): Show |
1 | a0001c0002t0001g0239 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-113+8733_-113+876 others(34): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595191 | ||||||
| chr18:66595235
|
C | A | 1 | a0001c0003t0004g0181 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-113+8719G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595235 | ||||||
| chr18:66595275
|
C | T | 1 | a0001c0024t0002g0134 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-113+8679G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595275 | ||||||
| chr18:66595445
|
GA | G | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+8508delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595445 | ||||||
| chr18:66595502
|
C | A | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+8452G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595502 | ||||||
| chr18:66595502
|
C | T | 183 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(180): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-113+8452G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595502 | ||||||
| chr18:66595512
|
G | GA | 52 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0203others(49): Show | 52 | HG00609.hp1 HG00735.hp1 HG01952.hp1 others(49): Show |
intron_variant | MODIFIER | c.-113+8441dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595512 | ||||||
| chr18:66595512
|
G | GAA | 6 | a0001c0001t0002g0215a0001c0001t0007g0213a0001c0001t0037g0212others(3): Show | 6 | HG02056.hp1 HG02109.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-113+8440_-113+844 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595512 | ||||||
| chr18:66595512
|
GA | G | 33 | a0001c0001t0002g0006a0001c0001t0002g0101a0001c0001t0002g0102others(30): Show | 33 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.-113+8441delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595512 | ||||||
| chr18:66595512
|
GAA | G | 6 | a0001c0001t0004g0007a0001c0001t0011g0236a0001c0001t0015g0237others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-113+8440_-113+844 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595512 | ||||||
| chr18:66595512
|
GAAA | G | 11 | a0001c0001t0002g0256a0001c0001t0002g0312a0001c0001t0003g0123others(8): Show | 11 | HG00558.hp1 HG02615.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-113+8439_-113+844 others(7): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595512 | ||||||
| chr18:66595512
|
GAAAA | G | 92 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0287others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.-113+8438_-113+844 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595512 | ||||||
| chr18:66595513
|
A | G | 1 | a0001c0001t0003g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-113+8441T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595513 | ||||||
| chr18:66595515
|
A | G | 1 | a0001c0001t0004g0007 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-113+8439T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595515 | ||||||
| chr18:66595747
|
C | T | 2 | a0001c0002t0001g0033a0001c0002t0008g0032 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-113+8207G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595747 | ||||||
| chr18:66595754
|
T | A | 1 | a0001c0002t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-113+8200A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595754 | ||||||
| chr18:66595779
|
A | C | 10 | a0001c0001t0003g0011a0001c0001t0004g0007a0001c0001t0006g0013others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-113+8175T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595779 | ||||||
| chr18:66595852
|
A | T | 16 | a0001c0001t0002g0287a0001c0001t0003g0265a0001c0001t0003g0313others(13): Show | 16 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-113+8102T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595852 | ||||||
| chr18:66595989
|
G | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+7965C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66595989 | ||||||
| chr18:66596120
|
T | C | 3 | a0001c0001t0011g0236a0001c0001t0015g0237a0004c0006t0014g0235 | 3 | HG01109.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-113+7834A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596120 | ||||||
| chr18:66596183
|
T | C | 1 | a0001c0002t0001g0318 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-113+7771A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596183 | ||||||
| chr18:66596415
|
G | T | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+7539C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596415 | ||||||
| chr18:66596506
|
G | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+7448C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596506 | ||||||
| chr18:66596509
|
C | A | 1 | a0001c0001t0003g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-113+7445G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596509 | ||||||
| chr18:66596582
|
C | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+7372G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596582 | ||||||
| chr18:66596785
|
A | T | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113+7169T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596785 | ||||||
| chr18:66596792
|
AT | A | 6 | a0001c0001t0006g0013a0001c0001t0010g0012a0001c0001t0010g0015others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113+7161delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596792 | ||||||
| chr18:66596820
|
C | T | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+7134G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596820 | ||||||
| chr18:66596834
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-113+7120C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596834 | ||||||
| chr18:66596858
|
G | A | 1 | a0001c0010t0001g0308 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-113+7096C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596858 | ||||||
| chr18:66596887
|
C | T | 1 | a0002c0004t0012g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-113+7067G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596887 | ||||||
| chr18:66596939
|
G | A | 156 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-113+7015C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596939 | ||||||
| chr18:66596950
|
C | T | 1 | a0001c0002t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-113+7004G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596950 | ||||||
| chr18:66596951
|
G | A | 67 | a0001c0001t0002g0034a0001c0001t0002g0044a0001c0001t0002g0051others(64): Show | 68 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.-113+7003C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66596951 | ||||||
| chr18:66597001
|
T | G | 1 | a0001c0001t0002g0006 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-113+6953A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597001 | ||||||
| chr18:66597009
|
G | A | 1 | a0014c0023t0004g0216 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-113+6945C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597009 | ||||||
| chr18:66597013
|
C | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+6941G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597013 | ||||||
| chr18:66597030
|
C | T | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+6924G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597030 | ||||||
| chr18:66597060
|
C | T | 6 | a0001c0010t0001g0280a0002c0004t0005g0275a0002c0004t0005g0276others(3): Show | 6 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113+6894G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597060 | ||||||
| chr18:66597061
|
G | A | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+6893C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597061 | ||||||
| chr18:66597081
|
C | CA | 13 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0003g0232others(10): Show | 13 | HG01978.hp2 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-113+6872dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597081 | ||||||
| chr18:66597081
|
C | CAA | 25 | a0001c0001t0002g0274a0001c0001t0003g0011a0001c0001t0003g0123others(22): Show | 25 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.-113+6871_-113+687 others(6): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597081 | ||||||
| chr18:66597081
|
C | CAAA | 97 | a0001c0001t0002g0026a0001c0001t0002g0254a0001c0001t0002g0287others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-113+6870_-113+687 others(7): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597081 | ||||||
| chr18:66597081
|
C | CAAAA | 57 | a0001c0001t0002g0034a0001c0001t0002g0044a0001c0001t0002g0051others(54): Show | 58 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-113+6869_-113+687 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597081 | ||||||
| chr18:66597081
|
C | CAAAAA | 18 | a0001c0001t0002g0068a0001c0001t0002g0101a0001c0001t0002g0102others(15): Show | 18 | HG00438.hp2 HG01884.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.-113+6868_-113+687 others(9): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597081 | ||||||
| chr18:66597081
|
CA | C | 8 | a0001c0001t0009g0130a0001c0001t0015g0246a0001c0002t0001g0129others(5): Show | 8 | HG01981.hp1 HG01981.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-113+6872delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597081 | ||||||
| chr18:66597162
|
T | TAAAAAAA others(4): Show |
12 | a0001c0001t0003g0265a0001c0001t0003g0270a0001c0001t0003g0271others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.-113+6781_-113+679 others(15): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597162 | ||||||
| chr18:66597162
|
T | TAAAAAAA others(5): Show |
79 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0287others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-113+6780_-113+679 others(16): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597162 | ||||||
| chr18:66597162
|
T | TAAAAAAA others(6): Show |
6 | a0001c0001t0002g0256a0001c0001t0003g0313a0001c0001t0004g0344others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-113+6779_-113+679 others(17): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597162 | ||||||
| chr18:66597162
|
T | TAAAAAAA others(8): Show |
1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-113+6777_-113+679 others(19): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597162 | ||||||
| chr18:66597162
|
TA | T | 41 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(38): Show | 41 | HG01074.hp1 HG01257.hp2 HG01258.hp2 others(38): Show |
intron_variant | MODIFIER | c.-113+6791delT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597162 | ||||||
| chr18:66597377
|
G | A | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+6577C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597377 | ||||||
| chr18:66597434
|
T | C | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113+6520A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597434 | ||||||
| chr18:66597479
|
A | T | 4 | a0001c0001t0003g0123a0001c0001t0038g0124a0001c0002t0001g0122others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+6475T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597479 | ||||||
| chr18:66597491
|
T | C | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+6463A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597491 | ||||||
| chr18:66597518
|
A | T | 1 | a0001c0002t0001g0239 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-113+6436T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597518 | ||||||
| chr18:66597593
|
G | A | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0083others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-113+6361C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597593 | ||||||
| chr18:66597596
|
A | G | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-113+6358T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597596 | ||||||
| chr18:66597690
|
C | T | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0083others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-113+6264G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597690 | ||||||
| chr18:66597704
|
G | A | 7 | a0001c0001t0003g0121a0001c0001t0009g0116a0001c0001t0009g0117others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+6250C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597704 | ||||||
| chr18:66597746
|
C | A | 3 | a0001c0001t0011g0236a0001c0001t0015g0237a0004c0006t0014g0235 | 3 | HG01109.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-113+6208G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597746 | ||||||
| chr18:66597795
|
G | T | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+6159C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597795 | ||||||
| chr18:66597867
|
G | A | 7 | a0001c0001t0003g0121a0001c0001t0009g0116a0001c0001t0009g0117others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+6087C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597867 | ||||||
| chr18:66597879
|
C | G | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+6075G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597879 | ||||||
| chr18:66597897
|
T | C | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+6057A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597897 | ||||||
| chr18:66597902
|
G | A | 6 | a0001c0001t0003g0315a0001c0001t0039g0319a0001c0002t0001g0316others(3): Show | 6 | HG00733.hp2 HG01433.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113+6052C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597902 | ||||||
| chr18:66597946
|
A | G | 2 | a0001c0003t0004g0019a0001c0003t0004g0020 | 2 | NA18952.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-113+6008T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66597946 | ||||||
| chr18:66598000
|
T | C | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+5954A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598000 | ||||||
| chr18:66598033
|
C | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+5921G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598033 | ||||||
| chr18:66598200
|
G | A | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+5754C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598200 | ||||||
| chr18:66598343
|
T | C | 7 | a0001c0001t0003g0121a0001c0001t0009g0116a0001c0001t0009g0117others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+5611A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598343 | ||||||
| chr18:66598366
|
C | G | 2 | a0003c0005t0022g0227a0003c0005t0043g0228 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-113+5588G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598366 | ||||||
| chr18:66598405
|
A | G | 1 | a0001c0003t0004g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-113+5549T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598405 | ||||||
| chr18:66598519
|
T | A | 1 | a0001c0001t0002g0321 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-113+5435A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598519 | ||||||
| chr18:66598704
|
G | A | 98 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+5250C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598704 | ||||||
| chr18:66598812
|
C | T | 7 | a0001c0001t0003g0121a0001c0001t0009g0116a0001c0001t0009g0117others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+5142G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598812 | ||||||
| chr18:66598871
|
T | G | 1 | a0003c0005t0022g0346 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-113+5083A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598871 | ||||||
| chr18:66598965
|
C | T | 18 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+4989G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66598965 | ||||||
| chr18:66599014
|
T | C | 7 | a0001c0001t0003g0121a0001c0001t0009g0116a0001c0001t0009g0117others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+4940A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66599014 | ||||||
| chr18:66599350
|
A | C | 10 | a0001c0001t0003g0011a0001c0001t0004g0007a0001c0001t0006g0013others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-113+4604T>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66599350 | ||||||
| chr18:66599680
|
A | G | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-113+4274T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66599680 | ||||||
| chr18:66599774
|
T | A | 1 | a0001c0001t0002g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-113+4180A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66599774 | ||||||
| chr18:66599843
|
G | T | 1 | a0001c0001t0006g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113+4111C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66599843 | ||||||
| chr18:66599907
|
G | C | 1 | a0001c0001t0009g0322 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-113+4047C>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66599907 | ||||||
| chr18:66600098
|
C | G | 7 | a0001c0001t0003g0121a0001c0001t0009g0116a0001c0001t0009g0117others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+3856G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600098 | ||||||
| chr18:66600372
|
T | C | 1 | a0001c0001t0004g0007 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-113+3582A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600372 | ||||||
| chr18:66600492
|
A | G | 1 | a0001c0001t0003g0114 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-113+3462T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600492 | ||||||
| chr18:66600540
|
G | A | 8 | a0001c0001t0003g0011a0001c0001t0006g0013a0001c0001t0010g0012others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-113+3414C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600540 | ||||||
| chr18:66600559
|
C | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(19): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-113+3395G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600559 | ||||||
| chr18:66600673
|
T | G | 30 | a0001c0001t0002g0333a0001c0001t0002g0334a0001c0001t0002g0335others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.-113+3281A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600673 | ||||||
| chr18:66600762
|
C | T | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113+3192G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600762 | ||||||
| chr18:66600763
|
G | T | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0083others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-113+3191C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600763 | ||||||
| chr18:66600918
|
G | A | 10 | a0001c0001t0003g0011a0001c0001t0004g0007a0001c0001t0006g0013others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-113+3036C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600918 | ||||||
| chr18:66600925
|
T | C | 2 | a0003c0005t0022g0227a0003c0005t0043g0228 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-113+3029A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600925 | ||||||
| chr18:66600973
|
C | G | 4 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(1): Show | 4 | NA18971.hp2 NA19006.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113+2981G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600973 | ||||||
| chr18:66600974
|
T | A | 4 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(1): Show | 4 | NA18971.hp2 NA19006.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113+2980A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600974 | ||||||
| chr18:66600984
|
G | A | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-113+2970C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66600984 | ||||||
| chr18:66601033
|
G | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+2921C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601033 | ||||||
| chr18:66601063
|
C | G | 1 | a0001c0001t0017g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-113+2891G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601063 | ||||||
| chr18:66601094
|
C | T | 1 | a0001c0002t0001g0074 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-113+2860G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601094 | ||||||
| chr18:66601262
|
T | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+2692A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601262 | ||||||
| chr18:66601290
|
A | G | 3 | a0001c0001t0011g0236a0001c0001t0015g0237a0004c0006t0014g0235 | 3 | HG01109.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-113+2664T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601290 | ||||||
| chr18:66601474
|
C | T | 7 | a0001c0002t0001g0258a0001c0002t0001g0259a0001c0002t0001g0260others(4): Show | 7 | NA18970.hp1 NA18971.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.-113+2480G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601474 | ||||||
| chr18:66601600
|
G | A | 1 | a0001c0001t0004g0007 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-113+2354C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601600 | ||||||
| chr18:66601651
|
A | G | 1 | a0001c0001t0002g0256 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-113+2303T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601651 | ||||||
| chr18:66601723
|
C | T | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+2231G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601723 | ||||||
| chr18:66601739
|
A | G | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+2215T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601739 | ||||||
| chr18:66601820
|
T | TA | 98 | a0001c0001t0002g0256a0001c0001t0002g0274a0001c0001t0002g0287others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-113+2133dupT | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601820 | ||||||
| chr18:66601900
|
C | T | 57 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0044others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113+2054G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601900 | ||||||
| chr18:66601922
|
G | A | 3 | a0001c0001t0011g0236a0001c0001t0015g0237a0004c0006t0014g0235 | 3 | HG01109.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-113+2032C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601922 | ||||||
| chr18:66601961
|
C | G | 1 | a0001c0003t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-113+1993G>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66601961 | ||||||
| chr18:66602068
|
G | T | 1 | a0002c0004t0005g0252 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-113+1886C>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602068 | ||||||
| chr18:66602088
|
T | A | 1 | a0002c0004t0012g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-113+1866A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602088 | ||||||
| chr18:66602558
|
T | C | 1 | a0001c0001t0003g0345 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-113+1396A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602558 | ||||||
| chr18:66602661
|
A | G | 1 | a0001c0001t0004g0007 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-113+1293T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602661 | ||||||
| chr18:66602699
|
T | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+1255A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602699 | ||||||
| chr18:66602754
|
AATTG | A | 4 | a0001c0001t0003g0249a0001c0001t0015g0246a0005c0009t0011g0247others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+1196_-113+119 others(8): Show |
CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602754 | ||||||
| chr18:66602756
|
T | C | 7 | a0001c0001t0003g0241a0001c0002t0001g0239a0001c0002t0001g0240others(4): Show | 7 | HG01070.hp1 HG01070.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+1198A>G | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602756 | ||||||
| chr18:66602914
|
G | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+1040C>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602914 | ||||||
| chr18:66602997
|
C | A | 1 | a0003c0005t0022g0346 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-113+957G>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66602997 | ||||||
| chr18:66603040
|
A | T | 2 | a0001c0001t0010g0250a0001c0001t0010g0251 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-113+914T>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66603040 | ||||||
| chr18:66603508
|
AT | A | 99 | a0001c0001t0002g0254a0001c0001t0002g0256a0001c0001t0002g0274others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.-113+445delA | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66603508 | ||||||
| chr18:66603595
|
C | T | 1 | a0002c0004t0005g0017 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-113+359G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66603595 | ||||||
| chr18:66603664
|
T | G | 1 | a0001c0001t0011g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-113+290A>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66603664 | ||||||
| chr18:66603784
|
C | T | 10 | a0001c0001t0003g0011a0001c0001t0004g0007a0001c0001t0006g0013others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-113+170G>A | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66603784 | ||||||
| chr18:66603818
|
T | A | 5 | a0001c0001t0002g0351a0001c0001t0002g0352a0001c0001t0003g0348others(2): Show | 5 | HG00408.hp1 HG02155.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-113+136A>T | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66603818 | ||||||
| chr18:66603883
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0002g0006 | 2 | NA18947.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-113+71T>C | CDH19 | ENSG00000071991.9 | transcript | ENST00000262150.7 | protein_coding | 1/11 | chr18 | 66603883 |