| geneid | 23500 |
|---|---|
| ensemblid | ENSG00000146122.17 |
| hgncid | 18143 |
| symbol | DAAM2 |
| name | dishevelled associated activator of morphogenesis 2 |
| refseq_nuc | NM_001201427.2 |
| refseq_prot | NP_001188356.1 |
| ensembl_nuc | ENST00000274867.9 |
| ensembl_prot | ENSP00000274867.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 39792376 |
| end | 39904869 |
| strand | + |
| ver | v1.2 |
| region | chr6:39792376-39904869 |
| region5000 | chr6:39787376-39909869 |
| regionname0 | DAAM2_chr6_39792376_39904869 |
| regionname5000 | DAAM2_chr6_39787376_39909869 |
| 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 | 1068 | 274 | 80 | 49 | 105 | 6 | 32 | 84 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0002 | 0/0 | 1068 | 6 | 0 | 0 | 5 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0003 | 0/0 | 1068 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0004 | 0/0 | 1068 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0005 | 0/0 | 1068 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0006 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0007 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0008 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0009 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0010 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0011 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0012 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0013 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0014 | 0/0 | 1068 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0015 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0016 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0017 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0018 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3207 | 94 | 18 | 22 | 30 | 5 | 18 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0002 | 1/0 | 3207 | 46 | 9 | 12 | 16 | 1 | 7 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0003 | 0/0 | 3207 | 38 | 7 | 9 | 20 | 0 | 2 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0004 | 0/0 | 3207 | 29 | 7 | 1 | 19 | 0 | 2 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0005 | 0/0 | 3207 | 12 | 6 | 0 | 6 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0006 | 0/0 | 3207 | 11 | 8 | 2 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0007 | 0/0 | 3207 | 10 | 0 | 0 | 10 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0008 | 0/0 | 3207 | 8 | 8 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0009 | 0/0 | 3207 | 4 | 4 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0010 | 0/0 | 3207 | 4 | 0 | 0 | 3 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0011 | 0/0 | 3207 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0012 | 0/0 | 3207 | 3 | 1 | 1 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0013 | 0/0 | 3207 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0014 | 0/0 | 3207 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0015 | 0/0 | 3207 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0016 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0017 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0018 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0019 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0020 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0021 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0022 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0023 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0024 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0025 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0026 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0027 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0028 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0029 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0030 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0031 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0032 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0033 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0034 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0035 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0036 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0037 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0038 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0039 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0040 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0041 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0042 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0043 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0044 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0045 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0046 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| c0047 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| 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 | 2979 | 100 | 30 | 22 | 26 | 2 | 19 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0002 | 1/0 | 2979 | 55 | 10 | 13 | 20 | 1 | 10 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0003 | 0/0 | 2983 | 39 | 6 | 6 | 26 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0004 | 0/0 | 2983 | 18 | 0 | 0 | 17 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0005 | 0/0 | 2983 | 8 | 8 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0006 | 0/0 | 2982 | 7 | 0 | 0 | 7 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0007 | 0/0 | 2983 | 6 | 0 | 5 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0008 | 0/0 | 2979 | 5 | 0 | 2 | 0 | 2 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0009 | 0/0 | 2979 | 5 | 5 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0010 | 0/0 | 2983 | 4 | 0 | 0 | 3 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0011 | 0/0 | 2979 | 4 | 4 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0012 | 0/0 | 2982 | 4 | 0 | 0 | 4 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0013 | 0/0 | 2982 | 4 | 0 | 0 | 4 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0014 | 0/0 | 2983 | 4 | 3 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0015 | 0/0 | 2982 | 3 | 0 | 0 | 3 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0016 | 0/0 | 2979 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0017 | 0/0 | 2979 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0018 | 0/0 | 2979 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0019 | 0/0 | 2979 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0020 | 0/0 | 2979 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0021 | 0/0 | 2979 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0022 | 0/0 | 2983 | 2 | 1 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0023 | 0/0 | 2983 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0024 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0025 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0026 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0027 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0028 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0029 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0030 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0031 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0032 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0033 | 0/0 | 2979 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0034 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0035 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0036 | 0/0 | 2979 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0037 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0038 | 0/0 | 2975 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0039 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| t0040 | 0/0 | 2979 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3207 | 94 | 18 | 22 | 30 | 5 | 18 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0002 | 1/0 | 3207 | 46 | 9 | 12 | 16 | 1 | 7 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0003 | 0/0 | 3207 | 38 | 7 | 9 | 20 | 0 | 2 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004 | 0/0 | 3207 | 29 | 7 | 1 | 19 | 0 | 2 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0005 | 0/0 | 3207 | 12 | 6 | 0 | 6 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0006 | 0/0 | 3207 | 11 | 8 | 2 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0007 | 0/0 | 3207 | 10 | 0 | 0 | 10 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0008 | 0/0 | 3207 | 8 | 8 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0009 | 0/0 | 3207 | 4 | 4 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0012 | 0/0 | 3207 | 3 | 1 | 1 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0013 | 0/0 | 3207 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0014 | 0/0 | 3207 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0016 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0017 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0022 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0025 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0026 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0031 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0032 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0033 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0036 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0037 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0039 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0042 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0044 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0045 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0046 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0002c0010 | 0/0 | 3207 | 4 | 0 | 0 | 3 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0002c0015 | 0/0 | 3207 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0003c0011 | 0/0 | 3207 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0003c0024 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0004c0020 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0004c0030 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0005c0023 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0006c0021 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0007c0018 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0008c0027 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0009c0041 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0010c0028 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0011c0029 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0012c0034 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0013c0038 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0014c0040 | 0/0 | 3207 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0015c0035 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0016c0043 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0017c0019 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0018c0047 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6185 | 78 | 14 | 19 | 26 | 2 | 16 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0001t0008 | 0/0 | 6185 | 5 | 0 | 2 | 0 | 2 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0001t0010 | 0/0 | 6189 | 4 | 0 | 0 | 3 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0001t0017 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0001t0019 | 0/0 | 6185 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0001t0025 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0001t0032 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0001t0033 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0001t0036 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0002t0002 | 1/0 | 6185 | 44 | 8 | 11 | 16 | 1 | 7 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0002t0030 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0002t0038 | 0/0 | 6181 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0003t0003 | 0/0 | 6189 | 29 | 2 | 6 | 20 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0003t0007 | 0/0 | 6189 | 3 | 0 | 3 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0003t0014 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0003t0016 | 0/0 | 6185 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0003t0039 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0003 | 0/0 | 6189 | 4 | 2 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0004 | 0/0 | 6189 | 12 | 0 | 0 | 11 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0006 | 0/0 | 6188 | 5 | 0 | 0 | 5 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0007 | 0/0 | 6189 | 2 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0012 | 0/0 | 6188 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0021 | 0/0 | 6185 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0026 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0031 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0004t0035 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0005t0003 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0005t0004 | 0/0 | 6189 | 4 | 0 | 0 | 4 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0005t0006 | 0/0 | 6188 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0005t0011 | 0/0 | 6185 | 4 | 4 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0005t0014 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0005t0037 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0006t0001 | 0/0 | 6185 | 8 | 5 | 2 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0006t0020 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0006t0027 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0006t0028 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0007t0003 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0007t0012 | 0/0 | 6188 | 3 | 0 | 0 | 3 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0007t0013 | 0/0 | 6188 | 4 | 0 | 0 | 4 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0007t0015 | 0/0 | 6188 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0008t0005 | 0/0 | 6189 | 7 | 7 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0008t0024 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0009t0009 | 0/0 | 6185 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0009t0029 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0012t0002 | 0/0 | 6185 | 3 | 1 | 1 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0013t0023 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0014t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0014t0017 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0016t0004 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0017t0018 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0022t0020 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0025t0034 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0026t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0031t0040 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0032t0009 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0033t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0036t0022 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0037t0002 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0039t0015 | 0/0 | 6188 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0042t0002 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0044t0022 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0045t0002 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0001c0046t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0002c0010t0002 | 0/0 | 6185 | 4 | 0 | 0 | 3 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0002c0015t0003 | 0/0 | 6189 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0003c0011t0001 | 0/0 | 6185 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0003c0024t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0004c0020t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0004c0030t0001 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0005c0023t0007 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0006c0021t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0007c0018t0018 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0008c0027t0006 | 0/0 | 6188 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0009c0041t0014 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0010c0028t0004 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0011c0029t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0012c0034t0001 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0013c0038t0009 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0014c0040t0002 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0015c0035t0003 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0016c0043t0005 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0017c0019t0003 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| a0018c0047t0001 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | copy fasta | chr6 | 39787376 | 39909869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0010g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0010g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0017g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0019g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0019g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0025g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0032g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0033g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0001t0036g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0002g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0030g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0002t0038g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0007g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0007g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0016g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0016g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0016g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0003t0039g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0007g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0021g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0021g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0026g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0031g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0004t0035g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0014g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0005t0037g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0020g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0027g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0006t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0012g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0013g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0013g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0013g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0013g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0007t0015g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0008t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0008t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0008t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0008t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0008t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0008t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0008t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0008t0024g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0009t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0009t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0009t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0009t0029g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0012t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0012t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0012t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0013t0023g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0013t0023g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0014t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0014t0017g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0016t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0017t0018g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0022t0020g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0025t0034g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0026t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0031t0040g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0032t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0033t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0036t0022g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0037t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0039t0015g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0042t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0044t0022g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0045t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0001c0046t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0002c0010t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0002c0010t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0002c0010t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0002c0010t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0002c0015t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0002c0015t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0003c0011t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0003c0011t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0003c0011t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0003c0024t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0004c0020t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0004c0030t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0005c0023t0007g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0006c0021t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0007c0018t0018g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0008c0027t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0009c0041t0014g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0010c0028t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0011c0029t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0012c0034t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0013c0038t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0014c0040t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0015c0035t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0016c0043t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0017c0019t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| a0018c0047t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0033 | g0226 | EUR | GBR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0156 | EUR | GBR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00323 | hp2 | a0001 | c0001 | t0008 | g0218 | EUR | FIN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00423 | hp1 | a0001 | c0003 | t0003 | g0059 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00423 | hp2 | a0001 | c0005 | t0006 | g0197 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00438 | hp1 | a0001 | c0003 | t0003 | g0108 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00438 | hp2 | a0002 | c0015 | t0003 | g0094 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00609 | hp1 | a0001 | c0004 | t0004 | g0195 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00621 | hp1 | a0001 | c0003 | t0003 | g0179 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0250 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00735 | hp1 | a0001 | c0004 | t0007 | g0157 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0215 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG00741 | hp2 | a0001 | c0006 | t0001 | g0158 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01074 | hp1 | a0001 | c0003 | t0007 | g0001 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01074 | hp2 | a0001 | c0002 | t0038 | g0130 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01081 | hp1 | a0004 | c0030 | t0001 | g0192 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0149 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01169 | hp2 | a0014 | c0040 | t0002 | g0230 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01175 | hp1 | a0001 | c0003 | t0007 | g0016 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01243 | hp1 | a0001 | c0031 | t0040 | g0143 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0254 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0146 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01358 | hp2 | a0001 | c0006 | t0001 | g0013 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01361 | hp2 | a0001 | c0044 | t0022 | g0114 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01433 | hp2 | a0001 | c0003 | t0007 | g0252 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0261 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0148 | EUR | IBS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01884 | hp1 | a0001 | c0026 | t0001 | g0280 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01884 | hp2 | a0001 | c0008 | t0005 | g0101 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01891 | hp1 | a0001 | c0013 | t0023 | g0170 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01934 | hp2 | a0005 | c0023 | t0007 | g0233 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0263 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0260 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0136 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01975 | hp1 | a0001 | c0003 | t0003 | g0035 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01978 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0257 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0145 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02004 | hp1 | a0001 | c0001 | t0036 | g0225 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0008 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02015 | hp2 | a0002 | c0010 | t0002 | g0255 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02027 | hp1 | a0002 | c0010 | t0002 | g0236 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02040 | hp2 | a0001 | c0003 | t0003 | g0103 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02055 | hp1 | a0001 | c0009 | t0009 | g0162 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02055 | hp2 | a0001 | c0008 | t0005 | g0286 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02056 | hp1 | a0002 | c0010 | t0002 | g0095 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02083 | hp1 | a0001 | c0003 | t0003 | g0287 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02083 | hp2 | a0001 | c0004 | t0004 | g0046 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02129 | hp1 | a0001 | c0004 | t0004 | g0070 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02129 | hp2 | a0002 | c0015 | t0003 | g0217 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02135 | hp1 | a0001 | c0003 | t0003 | g0268 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0176 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0191 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02257 | hp2 | a0001 | c0004 | t0003 | g0102 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02280 | hp1 | a0001 | c0005 | t0011 | g0124 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02280 | hp2 | a0001 | c0006 | t0001 | g0295 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02451 | hp1 | a0001 | c0004 | t0021 | g0100 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02523 | hp1 | a0001 | c0003 | t0003 | g0289 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02523 | hp2 | a0001 | c0001 | t0010 | g0084 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02572 | hp2 | a0001 | c0032 | t0009 | g0168 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02602 | hp1 | a0001 | c0001 | t0010 | g0269 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02615 | hp1 | a0001 | c0008 | t0024 | g0033 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02615 | hp2 | a0017 | c0019 | t0003 | g0036 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02622 | hp1 | a0001 | c0008 | t0005 | g0165 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02630 | hp1 | a0001 | c0009 | t0009 | g0111 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02630 | hp2 | a0001 | c0006 | t0001 | g0032 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02647 | hp1 | a0001 | c0004 | t0003 | g0115 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02683 | hp1 | a0018 | c0047 | t0001 | g0066 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02717 | hp1 | a0001 | c0003 | t0016 | g0284 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02735 | hp1 | a0001 | c0004 | t0007 | g0237 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02809 | hp2 | a0001 | c0002 | t0030 | g0174 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02818 | hp1 | a0001 | c0005 | t0014 | g0175 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02818 | hp2 | a0011 | c0029 | t0001 | g0177 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02886 | hp1 | a0001 | c0036 | t0022 | g0167 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02886 | hp2 | a0001 | c0006 | t0028 | g0187 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02895 | hp1 | a0001 | c0042 | t0002 | g0004 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02895 | hp2 | a0001 | c0006 | t0027 | g0188 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02922 | hp1 | a0003 | c0024 | t0001 | g0028 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0267 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02965 | hp1 | a0001 | c0005 | t0011 | g0042 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0190 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02970 | hp1 | a0003 | c0011 | t0001 | g0006 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02976 | hp1 | a0001 | c0004 | t0026 | g0027 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02976 | hp2 | a0001 | c0008 | t0005 | g0279 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03017 | hp1 | a0001 | c0003 | t0003 | g0199 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03041 | hp1 | a0001 | c0006 | t0001 | g0152 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03041 | hp2 | a0003 | c0011 | t0001 | g0005 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03098 | hp1 | a0001 | c0005 | t0003 | g0292 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03130 | hp1 | a0001 | c0005 | t0011 | g0092 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03130 | hp2 | a0001 | c0014 | t0017 | g0266 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03139 | hp1 | a0001 | c0009 | t0029 | g0173 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03139 | hp2 | a0001 | c0008 | t0005 | g0293 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0040 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03195 | hp2 | a0001 | c0009 | t0009 | g0128 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03209 | hp1 | a0001 | c0008 | t0005 | g0025 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03209 | hp2 | a0001 | c0033 | t0001 | g0044 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03225 | hp1 | a0016 | c0043 | t0005 | g0150 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03225 | hp2 | a0001 | c0014 | t0001 | g0029 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03453 | hp1 | a0001 | c0003 | t0014 | g0085 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0278 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03486 | hp1 | a0004 | c0020 | t0001 | g0277 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03486 | hp2 | a0001 | c0046 | t0001 | g0043 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03491 | hp1 | a0001 | c0045 | t0002 | g0163 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03516 | hp1 | a0003 | c0011 | t0001 | g0003 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03516 | hp2 | a0001 | c0004 | t0021 | g0060 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0121 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03540 | hp2 | a0001 | c0004 | t0035 | g0126 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0113 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0116 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0239 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03704 | hp1 | a0001 | c0037 | t0002 | g0214 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03704 | hp2 | a0001 | c0006 | t0001 | g0135 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03710 | hp1 | a0009 | c0041 | t0014 | g0147 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0132 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03927 | hp2 | a0002 | c0010 | t0002 | g0256 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG04184 | hp2 | a0001 | c0004 | t0004 | g0139 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG04199 | hp2 | a0001 | c0003 | t0039 | g0090 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0119 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG04228 | hp1 | a0012 | c0034 | t0001 | g0232 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0023 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0050 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18747 | hp1 | a0001 | c0007 | t0012 | g0078 | EAS | CHB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18747 | hp2 | a0001 | c0003 | t0003 | g0290 | EAS | CHB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18906 | hp1 | a0001 | c0022 | t0020 | g0047 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18939 | hp2 | a0001 | c0004 | t0006 | g0141 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18940 | hp2 | a0001 | c0003 | t0003 | g0068 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18944 | hp1 | a0010 | c0028 | t0004 | g0291 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18944 | hp2 | a0001 | c0007 | t0015 | g0245 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18945 | hp1 | a0001 | c0007 | t0013 | g0207 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18945 | hp2 | a0001 | c0004 | t0006 | g0089 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18949 | hp1 | a0008 | c0027 | t0006 | g0249 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18949 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0270 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18952 | hp2 | a0001 | c0005 | t0004 | g0081 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18954 | hp1 | a0001 | c0004 | t0004 | g0171 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18954 | hp2 | a0001 | c0007 | t0012 | g0079 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18956 | hp1 | a0001 | c0007 | t0013 | g0064 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18956 | hp2 | a0001 | c0004 | t0004 | g0051 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18960 | hp1 | a0001 | c0007 | t0003 | g0058 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18960 | hp2 | a0001 | c0004 | t0004 | g0061 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18963 | hp2 | a0001 | c0001 | t0032 | g0243 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18966 | hp2 | a0001 | c0007 | t0013 | g0246 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18968 | hp2 | a0001 | c0003 | t0003 | g0099 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18970 | hp1 | a0001 | c0003 | t0003 | g0083 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18970 | hp2 | a0001 | c0004 | t0003 | g0222 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18971 | hp2 | a0001 | c0004 | t0012 | g0098 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18975 | hp2 | a0001 | c0004 | t0006 | g0074 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18981 | hp1 | a0001 | c0007 | t0015 | g0057 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18984 | hp1 | a0001 | c0005 | t0004 | g0049 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18984 | hp2 | a0001 | c0003 | t0003 | g0014 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18990 | hp2 | a0001 | c0007 | t0012 | g0080 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18993 | hp1 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18994 | hp1 | a0015 | c0035 | t0003 | g0172 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18994 | hp2 | a0001 | c0016 | t0004 | g0054 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18997 | hp1 | a0001 | c0004 | t0004 | g0200 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18997 | hp2 | a0007 | c0018 | t0018 | g0053 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA18998 | hp2 | a0001 | c0004 | t0006 | g0288 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19002 | hp2 | a0001 | c0003 | t0003 | g0056 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19007 | hp1 | a0001 | c0004 | t0004 | g0091 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19009 | hp1 | a0001 | c0004 | t0004 | g0055 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19011 | hp2 | a0001 | c0005 | t0004 | g0212 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19030 | hp1 | a0001 | c0003 | t0016 | g0122 | AFR | LWK | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19030 | hp2 | a0001 | c0003 | t0014 | g0210 | AFR | LWK | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19043 | hp1 | a0001 | c0005 | t0011 | g0030 | AFR | LWK | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19060 | hp2 | a0001 | c0039 | t0015 | g0228 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19062 | hp1 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19066 | hp1 | a0001 | c0004 | t0004 | g0205 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19074 | hp2 | a0001 | c0007 | t0013 | g0082 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19077 | hp1 | a0001 | c0005 | t0037 | g0062 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19077 | hp2 | a0001 | c0005 | t0004 | g0063 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19079 | hp1 | a0001 | c0004 | t0003 | g0221 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19084 | hp1 | a0001 | c0004 | t0006 | g0142 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19084 | hp2 | a0001 | c0012 | t0002 | g0241 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19086 | hp1 | a0001 | c0004 | t0004 | g0037 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19086 | hp2 | a0001 | c0003 | t0003 | g0129 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19090 | hp2 | a0001 | c0003 | t0003 | g0110 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19091 | hp1 | a0001 | c0003 | t0003 | g0077 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19091 | hp2 | a0001 | c0017 | t0018 | g0052 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19240 | hp1 | a0001 | c0004 | t0031 | g0294 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA19240 | hp2 | a0001 | c0012 | t0002 | g0298 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | ASW | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA20129 | hp2 | a0001 | c0003 | t0016 | g0206 | AFR | ASW | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | GIH | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0264 | SAS | GIH | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01123 | hp1 | a0001 | c0012 | t0002 | g0219 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0159 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02109 | hp1 | a0001 | c0008 | t0005 | g0166 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02109 | hp2 | a0013 | c0038 | t0009 | g0041 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0276 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02486 | hp2 | a0001 | c0006 | t0020 | g0285 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02559 | hp1 | a0001 | c0013 | t0023 | g0169 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG03471 | hp2 | a0001 | c0001 | t0025 | g0031 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG06807 | hp1 | a0006 | c0021 | t0001 | g0297 | AFR | USA | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| HG06807 | hp2 | a0001 | c0025 | t0034 | g0300 | AFR | USA | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | USA | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0258 | REF | REF | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0299 | REF | REF | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:39792463
|
G | C | 1 | a0001 | 3 | HG02922.hp2 HG03130.hp2 NA19240.hp1 |
splice_region_variant | LOW | c.-59G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | chr6 | 39792463 | ||||||
| chr6:39856309
|
C | T | 1 | a0018 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.7C>T | p.Pro3Ser | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 153/6185 | 7/3207 | 3/1068 | chr6 | 39856309 | ||
| chr6:39856342
|
C | A | 1 | a0017 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.40C>A | p.Leu14Met | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 186/6185 | 40/3207 | 14/1068 | chr6 | 39856342 | ||
| chr6:39867596
|
G | A | 1 | a0005 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.515G>A | p.Arg172His | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/25 | 661/6185 | 515/3207 | 172/1068 | chr6 | 39867596 | ||
| chr6:39867706
|
C | T | 1 | a0006 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.625C>T | p.Arg209Cys | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/25 | 771/6185 | 625/3207 | 209/1068 | chr6 | 39867706 | ||
| chr6:39867814
|
G | C | 1 | a0003 | 4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.733G>C | p.Val245Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/25 | 879/6185 | 733/3207 | 245/1068 | chr6 | 39867814 | ||
| chr6:39867835
|
C | T | 1 | a0007 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.754C>T | p.Arg252Cys | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/25 | 900/6185 | 754/3207 | 252/1068 | chr6 | 39867835 | ||
| chr6:39875341
|
G | A | 1 | a0017 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1174G>A | p.Gly392Ser | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/25 | 1320/6185 | 1174/3207 | 392/1068 | chr6 | 39875341 | ||
| chr6:39878218
|
T | A | 1 | a0008 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1317T>A | p.Asn439Lys | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/25 | 1463/6185 | 1317/3207 | 439/1068 | chr6 | 39878218 | ||
| chr6:39879350
|
C | T | 1 | a0009 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1718C>T | p.Pro573Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/25 | 1864/6185 | 1718/3207 | 573/1068 | chr6 | 39879350 | ||
| chr6:39879422
|
G | A | 1 | a0010 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1790G>A | p.Arg597His | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/25 | 1936/6185 | 1790/3207 | 597/1068 | chr6 | 39879422 | ||
| chr6:39879422
|
G | C | 1 | a0011 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1790G>C | p.Arg597Pro | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/25 | 1936/6185 | 1790/3207 | 597/1068 | chr6 | 39879422 | ||
| chr6:39879431
|
A | G | 1 | a0002 | 6 | HG00438.hp2 HG02015.hp2 HG02027.hp1 others(3): Show |
missense_variant | MODERATE | c.1799A>G | p.Gln600Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/25 | 1945/6185 | 1799/3207 | 600/1068 | chr6 | 39879431 | ||
| chr6:39883966
|
G | A | 2 | a0004a0006 | 3 | HG01081.hp1 HG03486.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.1850G>A | p.Arg617His | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/25 | 1996/6185 | 1850/3207 | 617/1068 | chr6 | 39883966 | ||
| chr6:39884038
|
A | G | 1 | a0016 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1922A>G | p.Glu641Gly | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/25 | 2068/6185 | 1922/3207 | 641/1068 | chr6 | 39884038 | ||
| chr6:39891660
|
A | G | 1 | a0015 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.2279A>G | p.Gln760Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/25 | 2425/6185 | 2279/3207 | 760/1068 | chr6 | 39891660 | ||
| chr6:39901326
|
G | A | 1 | a0014 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.2836G>A | p.Gly946Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 24/25 | 2982/6185 | 2836/3207 | 946/1068 | chr6 | 39901326 | ||
| chr6:39901459
|
G | T | 1 | a0012 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2969G>T | p.Arg990Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 24/25 | 3115/6185 | 2969/3207 | 990/1068 | chr6 | 39901459 | ||
| chr6:39901990
|
G | A | 1 | a0013 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3160G>A | p.Ala1054Thr | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 3306/6185 | 3160/3207 | 1054/1068 | chr6 | 39901990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:39856329
|
T | C | 4 | a0001c0007a0001c0016a0001c0017others(1): Show | 13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
synonymous_variant | LOW | c.27T>C | p.His9His | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 173/6185 | 27/3207 | 9/1068 | chr6 | 39856329 | ||
| chr6:39856353
|
C | T | 1 | a0001c0046 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.51C>T | p.Phe17Phe | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 197/6185 | 51/3207 | 17/1068 | chr6 | 39856353 | ||
| chr6:39856431
|
G | A | 2 | a0004c0020a0006c0021 | 2 | HG03486.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.129G>A | p.Pro43Pro | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 275/6185 | 129/3207 | 43/1068 | chr6 | 39856431 | ||
| chr6:39856434
|
C | T | 1 | a0001c0045 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.132C>T | p.Asn44Asn | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 278/6185 | 132/3207 | 44/1068 | chr6 | 39856434 | ||
| chr6:39856449
|
C | T | 1 | a0001c0044 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.147C>T | p.Asn49Asn | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 293/6185 | 147/3207 | 49/1068 | chr6 | 39856449 | ||
| chr6:39860955
|
C | A | 1 | a0001c0022 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.196C>A | p.Arg66Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/25 | 342/6185 | 196/3207 | 66/1068 | chr6 | 39860955 | ||
| chr6:39868834
|
C | T | 3 | a0001c0008a0001c0046a0016c0043 | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
synonymous_variant | LOW | c.774C>T | p.Asn258Asn | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/25 | 920/6185 | 774/3207 | 258/1068 | chr6 | 39868834 | ||
| chr6:39875412
|
T | C | 3 | a0001c0013a0001c0025a0001c0026 | 4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
synonymous_variant | LOW | c.1245T>C | p.Gly415Gly | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/25 | 1391/6185 | 1245/3207 | 415/1068 | chr6 | 39875412 | ||
| chr6:39878206
|
C | T | 1 | a0001c0042 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1305C>T | p.Leu435Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/25 | 1451/6185 | 1305/3207 | 435/1068 | chr6 | 39878206 | ||
| chr6:39884042
|
G | A | 21 | a0001c0001a0001c0003a0001c0004others(18): Show | 181 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
synonymous_variant | LOW | c.1926G>A | p.Lys642Lys | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/25 | 2072/6185 | 1926/3207 | 642/1068 | chr6 | 39884042 | ||
| chr6:39887512
|
C | A | 12 | a0001c0003a0001c0008a0001c0009others(9): Show | 63 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(60): Show |
synonymous_variant | LOW | c.1980C>A | p.Ile660Ile | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/25 | 2126/6185 | 1980/3207 | 660/1068 | chr6 | 39887512 | ||
| chr6:39888745
|
T | A | 1 | a0001c0037 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2127T>A | p.Ala709Ala | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/25 | 2273/6185 | 2127/3207 | 709/1068 | chr6 | 39888745 | ||
| chr6:39896954
|
C | T | 19 | a0001c0001a0001c0006a0001c0008others(16): Show | 132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
synonymous_variant | LOW | c.2484C>T | p.Ile828Ile | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 20/25 | 2630/6185 | 2484/3207 | 828/1068 | chr6 | 39896954 | ||
| chr6:39897271
|
T | C | 40 | a0001c0001a0001c0003a0001c0004others(37): Show | 243 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
synonymous_variant | LOW | c.2607T>C | p.Ala869Ala | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/25 | 2753/6185 | 2607/3207 | 869/1068 | chr6 | 39897271 | ||
| chr6:39900178
|
G | T | 1 | a0001c0039 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.2781G>T | p.Leu927Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/25 | 2927/6185 | 2781/3207 | 927/1068 | chr6 | 39900178 | ||
| chr6:39901457
|
G | A | 1 | a0001c0033 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2967G>A | p.Ala989Ala | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 24/25 | 3113/6185 | 2967/3207 | 989/1068 | chr6 | 39901457 | ||
| chr6:39902007
|
G | T | 3 | a0001c0009a0001c0032a0013c0038 | 6 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.3177G>T | p.Arg1059Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 3323/6185 | 3177/3207 | 1059/1068 | chr6 | 39902007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:39792399
|
G | C | 3 | a0001c0001t0025a0001c0004t0026a0001c0008t0024 | 3 | HG02615.hp1 HG02976.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | 63904 | chr6 | 39792399 | |||||
| chr6:39792444
|
C | T | 1 | a0001c0031t0040 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | 63859 | chr6 | 39792444 | |||||
| chr6:39792455
|
G | A | 4 | a0001c0002t0030a0001c0006t0027a0001c0006t0028others(1): Show | 4 | HG02809.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | 63848 | chr6 | 39792455 | |||||
| chr6:39792460
|
C | T | 1 | a0001c0003t0039 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | 63843 | chr6 | 39792460 | |||||
| chr6:39902176
|
T | A | 36 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(33): Show | 139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*139T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 139 | chr6 | 39902176 | |||||
| chr6:39902237
|
T | C | 66 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(63): Show | 230 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*200T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 200 | chr6 | 39902237 | |||||
| chr6:39902253
|
C | T | 1 | a0001c0001t0036 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*216C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 216 | chr6 | 39902253 | |||||
| chr6:39902426
|
G | A | 4 | a0001c0004t0012a0001c0007t0012a0001c0017t0018others(1): Show | 6 | NA18747.hp1 NA18954.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*389G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 389 | chr6 | 39902426 | |||||
| chr6:39902491
|
C | A | 2 | a0001c0004t0021a0001c0004t0031 | 3 | HG02451.hp1 HG03516.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*454C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 454 | chr6 | 39902491 | |||||
| chr6:39902563
|
A | G | 1 | a0001c0005t0011 | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*526A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 526 | chr6 | 39902563 | |||||
| chr6:39902885
|
G | A | 1 | a0001c0001t0032 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 848 | chr6 | 39902885 | |||||
| chr6:39902930
|
T | A | 2 | a0001c0007t0015a0001c0039t0015 | 3 | NA18944.hp2 NA18981.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*893T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 893 | chr6 | 39902930 | |||||
| chr6:39902966
|
C | T | 4 | a0001c0009t0009a0001c0009t0029a0001c0032t0009others(1): Show | 6 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*929C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 929 | chr6 | 39902966 | |||||
| chr6:39902971
|
C | G | 2 | a0001c0007t0015a0001c0039t0015 | 3 | NA18944.hp2 NA18981.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*934C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 934 | chr6 | 39902971 | |||||
| chr6:39902975
|
G | C | 1 | a0001c0001t0033 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 938 | chr6 | 39902975 | |||||
| chr6:39903264
|
G | A | 1 | a0001c0013t0023 | 2 | HG01891.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1227G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1227 | chr6 | 39903264 | |||||
| chr6:39903435
|
T | C | 1 | a0001c0001t0019 | 2 | HG03540.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1398T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1398 | chr6 | 39903435 | |||||
| chr6:39903629
|
AC | A | 5 | a0001c0004t0012a0001c0007t0012a0001c0007t0013others(2): Show | 11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1594delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1594 | INFO_REALIGN_3_PRIME | chr6 | 39903629 | ||||
| chr6:39903748
|
CG | C | 3 | a0001c0004t0006a0001c0005t0006a0008c0027t0006 | 7 | HG00423.hp2 NA18939.hp2 NA18945.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1718delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1718 | INFO_REALIGN_3_PRIME | chr6 | 39903748 | ||||
| chr6:39903749
|
G | A | 5 | a0001c0004t0021a0001c0004t0031a0001c0006t0020others(2): Show | 6 | HG02451.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1712G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1712 | chr6 | 39903749 | |||||
| chr6:39903751
|
G | T | 4 | a0001c0003t0007a0001c0004t0007a0001c0004t0035others(1): Show | 7 | HG00735.hp1 HG01074.hp1 HG01175.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1714G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1714 | chr6 | 39903751 | |||||
| chr6:39903756
|
A | G | 8 | a0001c0003t0007a0001c0003t0014a0001c0003t0039others(5): Show | 12 | HG00735.hp1 HG01074.hp1 HG01175.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1719A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1719 | chr6 | 39903756 | |||||
| chr6:39903831
|
A | G | 2 | a0001c0036t0022a0001c0044t0022 | 2 | HG01361.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1794A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1794 | chr6 | 39903831 | |||||
| chr6:39904168
|
T | C | 5 | a0001c0004t0021a0001c0004t0031a0001c0006t0020others(2): Show | 6 | HG02451.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2131T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2131 | chr6 | 39904168 | |||||
| chr6:39904325
|
C | G | 1 | a0001c0025t0034 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2288C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2288 | chr6 | 39904325 | |||||
| chr6:39904429
|
G | C | 5 | a0001c0004t0021a0001c0004t0031a0001c0006t0020others(2): Show | 6 | HG02451.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2392G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2392 | chr6 | 39904429 | |||||
| chr6:39904448
|
T | C | 3 | a0001c0008t0005a0001c0008t0024a0016c0043t0005 | 9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2411T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2411 | chr6 | 39904448 | |||||
| chr6:39904464
|
C | G | 1 | a0001c0001t0008 | 5 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2427C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2427 | chr6 | 39904464 | |||||
| chr6:39904578
|
G | GAAAT | 40 | a0001c0001t0010a0001c0003t0003a0001c0003t0007others(37): Show | 111 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2545_*2548dupTAAA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2549 | INFO_REALIGN_3_PRIME | chr6 | 39904578 | ||||
| chr6:39904689
|
ACTAT | A | 6 | a0001c0002t0038a0001c0004t0021a0001c0004t0031others(3): Show | 7 | HG01074.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2659_*2662delATCT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2659 | INFO_REALIGN_3_PRIME | chr6 | 39904689 | ||||
| chr6:39904728
|
C | A | 28 | a0001c0001t0010a0001c0003t0003a0001c0003t0007others(25): Show | 78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2691C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2691 | chr6 | 39904728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:39792545
|
T | C | 1 | a0001c0003t0007g0001 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-57+80T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792545 | ||||||
| chr6:39792570
|
C | T | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+105C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792570 | ||||||
| chr6:39792670
|
G | C | 297 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.-57+205G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792670 | ||||||
| chr6:39792716
|
T | G | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 23 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+251T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792716 | ||||||
| chr6:39792797
|
G | A | 9 | a0001c0001t0025g0031a0001c0002t0002g0026a0001c0004t0026g0027others(6): Show | 9 | HG02615.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+332G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792797 | ||||||
| chr6:39792849
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+384T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792849 | ||||||
| chr6:39792937
|
G | A | 1 | a0001c0003t0003g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-57+472G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792937 | ||||||
| chr6:39792938
|
C | A | 1 | a0017c0019t0003g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57+473C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792938 | ||||||
| chr6:39792942
|
T | C | 1 | a0001c0008t0005g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-57+477T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792942 | ||||||
| chr6:39792965
|
A | G | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-57+500A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792965 | ||||||
| chr6:39793137
|
G | A | 1 | a0001c0003t0003g0110 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-57+672G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793137 | ||||||
| chr6:39793187
|
G | C | 1 | a0001c0009t0009g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57+722G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793187 | ||||||
| chr6:39793332
|
A | G | 1 | a0001c0002t0002g0296 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-57+867A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793332 | ||||||
| chr6:39793372
|
G | A | 1 | a0001c0004t0004g0037 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-57+907G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793372 | ||||||
| chr6:39793408
|
C | A | 1 | a0001c0003t0003g0002 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-57+943C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793408 | ||||||
| chr6:39793551
|
TC | T | 32 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-57+1089delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39793551 | |||||
| chr6:39793561
|
C | T | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+1096C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793561 | ||||||
| chr6:39793749
|
G | T | 5 | a0001c0003t0003g0287a0001c0003t0003g0289a0001c0003t0003g0290others(2): Show | 5 | HG02083.hp1 HG02523.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+1284G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793749 | ||||||
| chr6:39793820
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+1355G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793820 | ||||||
| chr6:39793960
|
T | A | 2 | a0001c0002t0002g0113a0001c0044t0022g0114 | 2 | HG01361.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57+1495T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793960 | ||||||
| chr6:39793995
|
G | T | 11 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0002t0002g0278others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+1530G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793995 | ||||||
| chr6:39794165
|
G | A | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+1700G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794165 | ||||||
| chr6:39794438
|
G | A | 32 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-57+1973G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794438 | ||||||
| chr6:39794568
|
A | G | 2 | a0001c0002t0002g0276a0004c0020t0001g0277 | 2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-57+2103A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794568 | ||||||
| chr6:39794726
|
C | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-57+2261C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794726 | ||||||
| chr6:39794797
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+2332G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794797 | ||||||
| chr6:39794884
|
C | T | 32 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-57+2419C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794884 | ||||||
| chr6:39794903
|
C | A | 3 | a0001c0003t0003g0116a0001c0004t0003g0115a0017c0019t0003g0036 | 3 | HG02615.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-57+2438C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794903 | ||||||
| chr6:39795206
|
T | A | 7 | a0001c0001t0001g0039a0001c0002t0002g0038a0001c0005t0011g0042others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+2741T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795206 | ||||||
| chr6:39795291
|
C | T | 11 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0010g0269others(8): Show | 11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+2826C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795291 | ||||||
| chr6:39795292
|
G | A | 20 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+2827G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795292 | ||||||
| chr6:39795348
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+2883A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795348 | ||||||
| chr6:39795419
|
G | C | 11 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0010g0269others(8): Show | 11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+2954G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795419 | ||||||
| chr6:39795439
|
G | A | 1 | a0001c0002t0002g0045 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-57+2974G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795439 | ||||||
| chr6:39795519
|
C | T | 2 | a0001c0001t0017g0267a0001c0014t0017g0266 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+3054C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795519 | ||||||
| chr6:39795730
|
T | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 107 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.-57+3265T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795730 | ||||||
| chr6:39796008
|
C | T | 3 | a0001c0001t0001g0265a0001c0002t0002g0263a0001c0002t0002g0264 | 3 | HG00735.hp2 HG01943.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-57+3543C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796008 | ||||||
| chr6:39796500
|
G | A | 2 | a0001c0001t0017g0267a0001c0014t0017g0266 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+4035G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796500 | ||||||
| chr6:39796548
|
T | C | 1 | a0001c0004t0003g0115 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57+4083T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796548 | ||||||
| chr6:39796594
|
T | C | 1 | a0001c0004t0004g0046 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-57+4129T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796594 | ||||||
| chr6:39796619
|
C | CA | 31 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 31 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+4176dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | |||||
| chr6:39796619
|
CA | C | 25 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0112others(22): Show | 25 | HG00438.hp1 HG00621.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.-57+4176delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | |||||
| chr6:39796619
|
CAA | C | 83 | a0001c0001t0001g0189a0001c0001t0001g0193a0001c0001t0001g0194others(80): Show | 83 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-57+4175_-57+4176d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | |||||
| chr6:39796619
|
CAAA | C | 13 | a0001c0001t0001g0259a0001c0001t0001g0272a0001c0001t0001g0273others(10): Show | 13 | HG01943.hp2 HG02083.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+4174_-57+4176d others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | |||||
| chr6:39796619
|
CAAAAA | C | 51 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0127others(48): Show | 51 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.-57+4172_-57+4176d others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | |||||
| chr6:39796619
|
CAAAAAA | C | 13 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0002t0002g0278others(10): Show | 13 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57+4171_-57+4176d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | |||||
| chr6:39796619
|
CAAAAAAA | C | 8 | a0001c0008t0005g0166a0001c0013t0023g0169a0001c0013t0023g0170others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+4170_-57+4176d others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | |||||
| chr6:39796646
|
TA | T | 213 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-57+4191delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796646 | |||||
| chr6:39796881
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57+4416T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796881 | ||||||
| chr6:39796930
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-57+4465T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796930 | ||||||
| chr6:39796957
|
C | T | 5 | a0001c0008t0005g0166a0001c0013t0023g0169a0001c0013t0023g0170others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+4492C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796957 | ||||||
| chr6:39796958
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+4493G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796958 | ||||||
| chr6:39797389
|
A | C | 1 | a0001c0001t0001g0258 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-57+4924A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797389 | ||||||
| chr6:39797443
|
A | G | 1 | a0001c0002t0002g0113 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+4978A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797443 | ||||||
| chr6:39797575
|
G | A | 5 | a0001c0001t0001g0193a0001c0002t0002g0191a0001c0003t0003g0176others(2): Show | 5 | HG01081.hp1 HG01243.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+5110G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797575 | ||||||
| chr6:39797617
|
C | T | 6 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0003t0003g0257others(3): Show | 6 | HG01257.hp1 HG01943.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+5152C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797617 | ||||||
| chr6:39797640
|
G | C | 1 | a0001c0004t0031g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57+5175G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797640 | ||||||
| chr6:39797701
|
C | G | 31 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 31 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+5236C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797701 | ||||||
| chr6:39797903
|
A | G | 2 | a0001c0001t0001g0251a0001c0003t0007g0252 | 2 | HG01175.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-57+5438A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797903 | ||||||
| chr6:39797921
|
A | G | 6 | a0001c0002t0002g0113a0001c0042t0002g0004a0001c0044t0022g0114others(3): Show | 6 | HG01361.hp2 HG02895.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+5456A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797921 | ||||||
| chr6:39798004
|
G | A | 1 | a0001c0001t0019g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57+5539G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798004 | ||||||
| chr6:39798016
|
C | T | 2 | a0001c0005t0003g0292a0001c0005t0014g0175 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-57+5551C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798016 | ||||||
| chr6:39798137
|
G | C | 11 | a0001c0002t0002g0113a0001c0008t0005g0166a0001c0013t0023g0169others(8): Show | 11 | HG01361.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+5672G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798137 | ||||||
| chr6:39798213
|
G | A | 2 | a0001c0008t0005g0166a0001c0036t0022g0167 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-57+5748G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798213 | ||||||
| chr6:39798279
|
C | T | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+5814C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798279 | ||||||
| chr6:39798302
|
A | G | 3 | a0001c0001t0001g0164a0001c0009t0009g0162a0001c0045t0002g0163 | 3 | HG02055.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+5837A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798302 | ||||||
| chr6:39798415
|
A | T | 4 | a0001c0042t0002g0004a0003c0011t0001g0003a0003c0011t0001g0005others(1): Show | 4 | HG02895.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+5950A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798415 | ||||||
| chr6:39798672
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+6207A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798672 | ||||||
| chr6:39798768
|
G | T | 5 | a0001c0008t0005g0166a0001c0013t0023g0169a0001c0013t0023g0170others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+6303G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798768 | ||||||
| chr6:39798871
|
AC | A | 59 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0127others(56): Show | 59 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-57+6407delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798871 | ||||||
| chr6:39799053
|
A | T | 3 | a0001c0003t0016g0284a0001c0006t0020g0285a0001c0008t0005g0286 | 3 | HG02055.hp2 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-57+6588A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799053 | ||||||
| chr6:39799062
|
G | A | 11 | a0001c0001t0001g0189a0001c0001t0001g0198a0001c0001t0001g0201others(8): Show | 11 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+6597G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799062 | ||||||
| chr6:39799064
|
G | T | 4 | a0001c0005t0011g0042a0001c0033t0001g0044a0001c0046t0001g0043others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+6599G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799064 | ||||||
| chr6:39799251
|
A | C | 1 | a0001c0009t0009g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57+6786A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799251 | ||||||
| chr6:39799286
|
G | T | 3 | a0001c0001t0001g0117a0001c0001t0019g0121a0001c0003t0016g0122 | 3 | HG02572.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-57+6821G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799286 | ||||||
| chr6:39799300
|
T | C | 1 | a0017c0019t0003g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57+6835T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799300 | ||||||
| chr6:39799361
|
C | T | 105 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(102): Show | 105 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.-57+6896C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799361 | ||||||
| chr6:39799411
|
G | A | 1 | a0001c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-57+6946G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799411 | ||||||
| chr6:39799421
|
G | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-57+6956G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799421 | ||||||
| chr6:39799448
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-57+6983A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799448 | ||||||
| chr6:39799466
|
T | G | 11 | a0001c0002t0002g0113a0001c0008t0005g0166a0001c0013t0023g0169others(8): Show | 11 | HG01361.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+7001T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799466 | ||||||
| chr6:39799481
|
G | A | 1 | a0001c0004t0004g0171 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-57+7016G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799481 | ||||||
| chr6:39799514
|
A | C | 2 | a0001c0002t0002g0113a0001c0044t0022g0114 | 2 | HG01361.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57+7049A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799514 | ||||||
| chr6:39799535
|
T | C | 95 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0065others(92): Show | 95 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-57+7070T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799535 | ||||||
| chr6:39799762
|
C | A | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+7297C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799762 | ||||||
| chr6:39799767
|
G | A | 5 | a0001c0008t0005g0166a0001c0013t0023g0169a0001c0013t0023g0170others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+7302G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799767 | ||||||
| chr6:39799964
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-57+7499A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799964 | ||||||
| chr6:39800229
|
G | T | 105 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0182others(102): Show | 105 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-57+7764G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800229 | ||||||
| chr6:39800233
|
T | C | 1 | a0001c0002t0002g0113 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+7768T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800233 | ||||||
| chr6:39800247
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0019g0121others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7782G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800247 | ||||||
| chr6:39800493
|
A | G | 3 | a0001c0001t0001g0164a0001c0009t0009g0162a0001c0045t0002g0163 | 3 | HG02055.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+8028A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800493 | ||||||
| chr6:39800631
|
G | A | 210 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-57+8166G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800631 | ||||||
| chr6:39800639
|
G | A | 1 | a0004c0020t0001g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+8174G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800639 | ||||||
| chr6:39800660
|
C | T | 6 | a0001c0002t0030g0174a0001c0005t0003g0292a0001c0005t0014g0175others(3): Show | 6 | HG02809.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+8195C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800660 | ||||||
| chr6:39800743
|
G | A | 1 | a0001c0002t0002g0113 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+8278G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800743 | ||||||
| chr6:39800743
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-57+8278G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800743 | ||||||
| chr6:39800763
|
C | T | 5 | a0001c0002t0002g0159a0001c0042t0002g0004a0003c0011t0001g0003others(2): Show | 5 | HG01123.hp2 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+8298C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800763 | ||||||
| chr6:39801153
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0019g0050 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57+8688A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801153 | ||||||
| chr6:39801218
|
A | G | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+8753A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801218 | ||||||
| chr6:39801296
|
C | T | 1 | a0001c0006t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-57+8831C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801296 | ||||||
| chr6:39801495
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57+9030C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801495 | ||||||
| chr6:39801528
|
T | C | 106 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(103): Show | 106 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.-57+9063T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801528 | ||||||
| chr6:39801609
|
T | C | 211 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-57+9144T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801609 | ||||||
| chr6:39801679
|
C | T | 106 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0182others(103): Show | 106 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-57+9214C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801679 | ||||||
| chr6:39801809
|
G | C | 3 | a0001c0001t0001g0117a0001c0001t0019g0121a0001c0003t0016g0122 | 3 | HG02572.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-57+9344G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801809 | ||||||
| chr6:39801813
|
A | G | 1 | a0001c0003t0003g0103 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-57+9348A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801813 | ||||||
| chr6:39801818
|
T | C | 211 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-57+9353T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801818 | ||||||
| chr6:39801853
|
A | C | 2 | a0001c0001t0001g0164a0001c0045t0002g0163 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+9388A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801853 | ||||||
| chr6:39801861
|
G | A | 20 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+9396G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801861 | ||||||
| chr6:39802027
|
A | T | 211 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-57+9562A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802027 | ||||||
| chr6:39802166
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+9701G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802166 | ||||||
| chr6:39802388
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0019g0121others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+9923G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802388 | ||||||
| chr6:39802597
|
C | G | 3 | a0001c0001t0001g0024a0001c0002t0002g0156a0001c0004t0007g0157 | 3 | HG00099.hp2 HG00735.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-57+10132C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802597 | ||||||
| chr6:39802666
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-57+10201G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802666 | ||||||
| chr6:39802769
|
A | G | 2 | a0001c0002t0002g0038a0001c0006t0001g0040 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-57+10304A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802769 | ||||||
| chr6:39802775
|
G | C | 210 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-57+10310G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802775 | ||||||
| chr6:39802834
|
C | T | 1 | a0001c0009t0009g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57+10369C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802834 | ||||||
| chr6:39802865
|
C | T | 11 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0010g0269others(8): Show | 11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+10400C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802865 | ||||||
| chr6:39803096
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0019g0121others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+10631G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803096 | ||||||
| chr6:39803180
|
G | A | 214 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-57+10715G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803180 | ||||||
| chr6:39803194
|
A | G | 6 | a0001c0002t0002g0113a0001c0042t0002g0004a0001c0044t0022g0114others(3): Show | 6 | HG01361.hp2 HG02895.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+10729A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803194 | ||||||
| chr6:39803394
|
G | T | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0002t0002g0278others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+10929G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803394 | ||||||
| chr6:39803478
|
A | G | 1 | a0001c0002t0002g0250 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-57+11013A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803478 | ||||||
| chr6:39803514
|
T | C | 210 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-57+11049T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803514 | ||||||
| chr6:39803664
|
T | G | 9 | a0001c0002t0002g0113a0001c0013t0023g0169a0001c0013t0023g0170others(6): Show | 9 | HG01361.hp2 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+11199T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803664 | ||||||
| chr6:39803764
|
G | T | 2 | a0001c0001t0001g0112a0001c0009t0009g0111 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-57+11299G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803764 | ||||||
| chr6:39803831
|
C | A | 1 | a0001c0002t0002g0261 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-57+11366C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803831 | ||||||
| chr6:39803836
|
T | C | 1 | a0001c0003t0016g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-57+11371T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803836 | ||||||
| chr6:39803938
|
G | C | 1 | a0001c0009t0009g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57+11473G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803938 | ||||||
| chr6:39803968
|
T | C | 3 | a0001c0001t0001g0164a0001c0009t0009g0162a0001c0045t0002g0163 | 3 | HG02055.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+11503T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803968 | ||||||
| chr6:39804039
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-57+11574C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804039 | ||||||
| chr6:39804065
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+11600G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804065 | ||||||
| chr6:39804180
|
C | T | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-57+11715C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804180 | ||||||
| chr6:39804208
|
C | T | 2 | a0001c0001t0001g0022a0001c0002t0002g0021 | 2 | HG00323.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-57+11743C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804208 | ||||||
| chr6:39804258
|
C | A | 210 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-57+11793C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804258 | ||||||
| chr6:39804349
|
G | A | 11 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0002t0002g0278others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+11884G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804349 | ||||||
| chr6:39804371
|
CTGTA | C | 14 | a0001c0001t0001g0164a0001c0001t0001g0281a0001c0001t0001g0282others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+11912_-57+1191 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804371 | |||||
| chr6:39804447
|
A | G | 2 | a0001c0001t0001g0112a0001c0009t0009g0111 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-57+11982A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804447 | ||||||
| chr6:39804522
|
C | CTG | 90 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0034others(87): Show | 90 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-57+12087_-57+1208 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | |||||
| chr6:39804522
|
C | CTGTG | 56 | a0001c0001t0001g0112a0001c0001t0001g0118a0001c0001t0001g0178others(53): Show | 56 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.-57+12085_-57+1208 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | |||||
| chr6:39804522
|
C | CTGTGTG | 26 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0198others(23): Show | 26 | HG00423.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-57+12083_-57+1208 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | |||||
| chr6:39804522
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0117a0001c0001t0001g0201a0001c0001t0001g0259others(4): Show | 7 | HG02572.hp1 HG02738.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+12081_-57+1208 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | |||||
| chr6:39804522
|
CTG | C | 16 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0010g0269others(13): Show | 16 | HG01891.hp1 HG02083.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57+12087_-57+1208 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | |||||
| chr6:39804522
|
CTGTG | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01255.hp1 HG01358.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+12085_-57+1208 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | |||||
| chr6:39804583
|
G | A | 1 | a0001c0004t0026g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-57+12118G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804583 | ||||||
| chr6:39804677
|
T | A | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-57+12212T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804677 | ||||||
| chr6:39804692
|
C | T | 2 | a0001c0004t0021g0100a0001c0008t0005g0101 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-57+12227C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804692 | ||||||
| chr6:39804754
|
GTGGTACC others(4): Show |
G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12292_-57+1230 others(15): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804754 | |||||
| chr6:39804769
|
A | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12304A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804769 | ||||||
| chr6:39804770
|
G | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12305G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804770 | ||||||
| chr6:39804778
|
G | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12313G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804778 | ||||||
| chr6:39804779
|
A | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12314A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804779 | ||||||
| chr6:39804781
|
G | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12316G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804781 | ||||||
| chr6:39804782
|
G | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12317G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804782 | ||||||
| chr6:39804788
|
A | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12323A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804788 | ||||||
| chr6:39804791
|
A | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12326A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804791 | ||||||
| chr6:39804793
|
A | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12328A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804793 | ||||||
| chr6:39804797
|
A | C | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12332A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804797 | ||||||
| chr6:39804799
|
A | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12334A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804799 | ||||||
| chr6:39804800
|
G | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12335G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804800 | ||||||
| chr6:39804801
|
T | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12336T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804801 | ||||||
| chr6:39804802
|
G | A | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12337G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804802 | ||||||
| chr6:39804803
|
C | A | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12338C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804803 | ||||||
| chr6:39804810
|
C | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12345C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804810 | ||||||
| chr6:39804831
|
T | A | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12366T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804831 | ||||||
| chr6:39804834
|
T | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12369T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804834 | ||||||
| chr6:39804838
|
T | A | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12373T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804838 | ||||||
| chr6:39804842
|
A | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12377A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804842 | ||||||
| chr6:39804850
|
T | A | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12385T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804850 | ||||||
| chr6:39804863
|
A | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12398A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804863 | ||||||
| chr6:39804868
|
C | A | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12403C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804868 | ||||||
| chr6:39804883
|
G | A | 3 | a0001c0001t0001g0106a0001c0017t0018g0052a0007c0018t0018g0053 | 3 | NA18988.hp2 NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-57+12418G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804883 | ||||||
| chr6:39804915
|
T | C | 2 | a0001c0001t0001g0164a0001c0045t0002g0163 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+12450T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804915 | ||||||
| chr6:39804923
|
A | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12458A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804923 | ||||||
| chr6:39804928
|
G | GGTCTGGT others(26): Show |
1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12465_-57+1246 others(37): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804928 | |||||
| chr6:39804943
|
C | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12478C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804943 | ||||||
| chr6:39804947
|
C | A | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12482C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804947 | ||||||
| chr6:39804948
|
A | C | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12483A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804948 | ||||||
| chr6:39804949
|
C | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12484C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804949 | ||||||
| chr6:39804964
|
T | C | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12499T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804964 | ||||||
| chr6:39804980
|
TGACTGCA others(14): Show |
T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12516_-57+1253 others(25): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804980 | ||||||
| chr6:39805005
|
T | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12540T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805005 | ||||||
| chr6:39805009
|
T | A | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12544T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805009 | ||||||
| chr6:39805033
|
G | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12568G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805033 | ||||||
| chr6:39805034
|
A | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12569A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805034 | ||||||
| chr6:39805035
|
A | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12570A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805035 | ||||||
| chr6:39805037
|
C | G | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12572C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805037 | ||||||
| chr6:39805038
|
A | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12573A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805038 | ||||||
| chr6:39805105
|
A | G | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+12640A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805105 | ||||||
| chr6:39805117
|
G | A | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+12652G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805117 | ||||||
| chr6:39805221
|
C | G | 3 | a0001c0003t0003g0116a0001c0004t0003g0115a0017c0019t0003g0036 | 3 | HG02615.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-57+12756C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805221 | ||||||
| chr6:39805297
|
T | A | 108 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0182others(105): Show | 108 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-57+12832T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805297 | ||||||
| chr6:39805407
|
A | G | 1 | a0001c0004t0007g0237 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-57+12942A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805407 | ||||||
| chr6:39805557
|
A | AT | 13 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0248others(10): Show | 13 | HG01361.hp2 HG01891.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+13107dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39805557 | |||||
| chr6:39805557
|
AT | A | 55 | a0001c0001t0001g0024a0001c0001t0001g0112a0001c0001t0001g0123others(52): Show | 55 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.-57+13107delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39805557 | |||||
| chr6:39805617
|
C | G | 1 | a0001c0005t0011g0124 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57+13152C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805617 | ||||||
| chr6:39805715
|
C | T | 1 | a0001c0006t0001g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-57+13250C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805715 | ||||||
| chr6:39805841
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+13376C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805841 | ||||||
| chr6:39805908
|
C | T | 1 | a0001c0005t0011g0124 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57+13443C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805908 | ||||||
| chr6:39806030
|
G | C | 1 | a0001c0016t0004g0054 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-57+13565G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806030 | ||||||
| chr6:39806197
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57+13732C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806197 | ||||||
| chr6:39806515
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57+14050C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806515 | ||||||
| chr6:39806686
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-57+14221C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806686 | ||||||
| chr6:39806792
|
C | T | 3 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0032t0009g0168 | 3 | HG01891.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-57+14327C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806792 | ||||||
| chr6:39806840
|
C | CA | 10 | a0001c0001t0001g0106a0001c0003t0003g0056a0001c0003t0003g0059others(7): Show | 10 | HG00423.hp1 HG02818.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57+14390dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39806840 | |||||
| chr6:39806854
|
AAG | A | 15 | a0001c0001t0001g0201a0001c0001t0001g0281a0001c0001t0001g0282others(12): Show | 15 | HG01884.hp1 HG01891.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57+14391_-57+1439 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39806854 | |||||
| chr6:39806855
|
AG | A | 184 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-57+14391delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806855 | ||||||
| chr6:39806856
|
G | A | 13 | a0001c0001t0001g0178a0001c0001t0001g0211a0001c0001t0001g0251others(10): Show | 13 | HG00642.hp2 HG01175.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57+14391G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806856 | ||||||
| chr6:39806917
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+14452A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806917 | ||||||
| chr6:39806967
|
C | T | 1 | a0001c0004t0012g0098 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-57+14502C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806967 | ||||||
| chr6:39807183
|
C | T | 3 | a0001c0006t0001g0152a0001c0006t0001g0158a0001c0008t0005g0165 | 3 | HG00741.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-57+14718C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807183 | ||||||
| chr6:39807188
|
C | CA | 9 | a0001c0001t0001g0213a0001c0001t0001g0274a0001c0002t0002g0253others(6): Show | 9 | HG00741.hp2 HG01981.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+14737dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39807188 | |||||
| chr6:39807188
|
CA | C | 115 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0065others(112): Show | 115 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-57+14737delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39807188 | |||||
| chr6:39807188
|
CAA | C | 8 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0019g0050others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+14736_-57+1473 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39807188 | |||||
| chr6:39807199
|
A | G | 2 | a0001c0001t0017g0267a0001c0014t0017g0266 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+14734A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807199 | ||||||
| chr6:39807205
|
G | A | 64 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-57+14740G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807205 | ||||||
| chr6:39807239
|
A | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0026t0001g0280 | 3 | HG01884.hp1 HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-57+14774A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807239 | ||||||
| chr6:39807371
|
C | A | 2 | a0001c0001t0017g0267a0001c0014t0017g0266 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+14906C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807371 | ||||||
| chr6:39807458
|
A | G | 209 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-57+14993A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807458 | ||||||
| chr6:39807479
|
G | A | 3 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0032t0009g0168 | 3 | HG01891.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-57+15014G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807479 | ||||||
| chr6:39807532
|
T | C | 1 | a0001c0004t0004g0061 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-57+15067T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807532 | ||||||
| chr6:39807541
|
G | C | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57+15076G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807541 | ||||||
| chr6:39807578
|
G | A | 15 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0010g0269others(12): Show | 15 | HG02083.hp1 HG02109.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57+15113G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807578 | ||||||
| chr6:39807603
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-57+15138G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807603 | ||||||
| chr6:39807828
|
T | C | 4 | a0001c0042t0002g0004a0003c0011t0001g0003a0003c0011t0001g0005others(1): Show | 4 | HG02895.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+15363T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807828 | ||||||
| chr6:39807874
|
G | C | 1 | a0001c0008t0005g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-57+15409G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807874 | ||||||
| chr6:39808039
|
A | G | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+15574A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808039 | ||||||
| chr6:39808075
|
C | CT | 9 | a0001c0001t0001g0096a0001c0001t0001g0213a0001c0001t0001g0259others(6): Show | 9 | HG00423.hp1 HG01891.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+15626dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39808075 | |||||
| chr6:39808075
|
CT | C | 8 | a0001c0001t0008g0215a0001c0001t0017g0267a0001c0002t0002g0238others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+15626delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39808075 | |||||
| chr6:39808075
|
CTT | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.-57+15625_-57+1562 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39808075 | |||||
| chr6:39808100
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-57+15635C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808100 | ||||||
| chr6:39808177
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-57+15712A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808177 | ||||||
| chr6:39808404
|
A | G | 112 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0182others(109): Show | 112 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-57+15939A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808404 | ||||||
| chr6:39808498
|
C | T | 1 | a0001c0006t0001g0013 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-57+16033C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808498 | ||||||
| chr6:39808584
|
C | A | 194 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0034others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-57+16119C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808584 | ||||||
| chr6:39808613
|
G | A | 1 | a0002c0015t0003g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-57+16148G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808613 | ||||||
| chr6:39808620
|
C | T | 3 | a0001c0003t0016g0284a0001c0006t0020g0285a0001c0008t0005g0286 | 3 | HG02055.hp2 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-57+16155C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808620 | ||||||
| chr6:39808773
|
G | T | 1 | a0001c0008t0005g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-57+16308G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808773 | ||||||
| chr6:39808893
|
A | C | 1 | a0001c0002t0002g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-57+16428A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808893 | ||||||
| chr6:39808996
|
A | G | 3 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0032t0009g0168 | 3 | HG01891.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-57+16531A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808996 | ||||||
| chr6:39809103
|
C | G | 3 | a0001c0003t0003g0116a0001c0004t0003g0115a0017c0019t0003g0036 | 3 | HG02615.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-57+16638C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809103 | ||||||
| chr6:39809259
|
G | A | 1 | a0001c0003t0003g0103 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-57+16794G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809259 | ||||||
| chr6:39809362
|
C | T | 1 | a0001c0002t0002g0097 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-57+16897C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809362 | ||||||
| chr6:39809434
|
C | T | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+16969C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809434 | ||||||
| chr6:39809435
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-57+16970G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809435 | ||||||
| chr6:39809595
|
G | T | 3 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0032t0009g0168 | 3 | HG01891.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-57+17130G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809595 | ||||||
| chr6:39809668
|
A | G | 3 | a0001c0001t0001g0164a0001c0009t0009g0162a0001c0045t0002g0163 | 3 | HG02055.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+17203A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809668 | ||||||
| chr6:39809939
|
C | G | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 90 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-57+17474C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809939 | ||||||
| chr6:39810116
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57+17651G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810116 | ||||||
| chr6:39810131
|
T | C | 2 | a0001c0001t0017g0267a0001c0014t0017g0266 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+17666T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810131 | ||||||
| chr6:39810461
|
T | G | 296 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-57+17996T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810461 | ||||||
| chr6:39810635
|
G | A | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-57+18170G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810635 | ||||||
| chr6:39810733
|
G | A | 1 | a0001c0002t0002g0253 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-57+18268G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810733 | ||||||
| chr6:39810742
|
T | G | 1 | a0001c0004t0004g0055 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-57+18277T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810742 | ||||||
| chr6:39810838
|
A | G | 2 | a0001c0002t0002g0296a0001c0003t0003g0196 | 2 | NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-57+18373A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810838 | ||||||
| chr6:39810863
|
C | T | 1 | a0001c0001t0017g0267 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-57+18398C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810863 | ||||||
| chr6:39811033
|
A | G | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+18568A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811033 | ||||||
| chr6:39811174
|
A | AGT | 55 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0067others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.-57+18747_-57+1874 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
A | AGTAT | 4 | a0001c0002t0030g0174a0001c0006t0027g0188a0001c0006t0028g0187others(1): Show | 4 | HG02809.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+18711_-57+1871 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
A | AGTGT | 16 | a0001c0001t0001g0093a0001c0001t0001g0109a0001c0001t0001g0151others(13): Show | 16 | HG00438.hp2 HG02602.hp1 HG02735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+18745_-57+1874 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
A | AGTGTGT | 16 | a0001c0001t0001g0104a0001c0001t0001g0164a0001c0001t0001g0235others(13): Show | 16 | HG02056.hp1 HG02083.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+18743_-57+1874 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
A | AGTGTGTG others(1): Show |
10 | a0001c0001t0001g0112a0001c0001t0001g0272a0001c0002t0002g0023others(7): Show | 10 | HG02280.hp2 HG02486.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57+18741_-57+1874 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
A | AGTGTGTG others(3): Show |
7 | a0001c0001t0017g0267a0001c0002t0002g0019a0001c0002t0002g0020others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+18739_-57+1874 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
AGT | A | 10 | a0001c0002t0002g0107a0001c0003t0003g0129a0001c0004t0031g0294others(7): Show | 10 | HG01358.hp2 HG01361.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57+18747_-57+1874 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
AGTGT | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00323.hp1 HG00621.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+18745_-57+1874 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0001g0234a0005c0023t0007g0233 | 2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-57+18735_-57+1874 others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811174
|
AGTGTGTG others(9): Show |
A | 87 | a0001c0001t0001g0034a0001c0001t0001g0178a0001c0001t0001g0181others(84): Show | 87 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-57+18733_-57+1874 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | |||||
| chr6:39811466
|
A | C | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0003t0007g0016 | 3 | HG01175.hp1 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-57+19001A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811466 | ||||||
| chr6:39811488
|
T | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp1 HG00621.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57+19023T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811488 | ||||||
| chr6:39811528
|
C | T | 6 | a0001c0001t0001g0193a0001c0002t0002g0191a0001c0003t0003g0176others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+19063C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811528 | ||||||
| chr6:39811549
|
G | A | 48 | a0001c0001t0001g0024a0001c0001t0001g0127a0001c0001t0001g0131others(45): Show | 48 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-57+19084G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811549 | ||||||
| chr6:39811564
|
C | A | 2 | a0001c0001t0019g0121a0001c0003t0016g0122 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-57+19099C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811564 | ||||||
| chr6:39811750
|
A | C | 243 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0039others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.-57+19285A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811750 | ||||||
| chr6:39811819
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-57+19354C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811819 | ||||||
| chr6:39811940
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57+19475C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811940 | ||||||
| chr6:39811955
|
T | A | 1 | a0001c0002t0038g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-57+19490T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811955 | ||||||
| chr6:39811956
|
G | T | 4 | a0001c0042t0002g0004a0003c0011t0001g0003a0003c0011t0001g0005others(1): Show | 4 | HG02895.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+19491G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811956 | ||||||
| chr6:39812050
|
G | T | 63 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0127others(60): Show | 63 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-57+19585G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812050 | ||||||
| chr6:39812086
|
A | C | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 94 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.-57+19621A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812086 | ||||||
| chr6:39812128
|
C | T | 37 | a0001c0001t0001g0024a0001c0001t0001g0127a0001c0001t0001g0134others(34): Show | 37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-57+19663C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812128 | ||||||
| chr6:39812339
|
C | G | 1 | a0001c0008t0005g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-57+19874C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812339 | ||||||
| chr6:39812390
|
T | C | 1 | a0001c0009t0009g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57+19925T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812390 | ||||||
| chr6:39812472
|
G | A | 24 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0211others(21): Show | 24 | HG00323.hp2 HG00741.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.-57+20007G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812472 | ||||||
| chr6:39812551
|
T | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00323.hp1 HG00621.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-57+20086T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812551 | ||||||
| chr6:39812586
|
C | T | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+20121C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812586 | ||||||
| chr6:39812617
|
ATTC | A | 42 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0127others(39): Show | 42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+20155_-57+2015 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39812617 | |||||
| chr6:39812646
|
G | GTGGAGTC others(13): Show |
39 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0127others(36): Show | 39 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.-57+20189_-57+2019 others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39812646 | |||||
| chr6:39812646
|
G | GTGGAGTC others(13): Show |
3 | a0001c0001t0001g0164a0001c0005t0011g0124a0001c0045t0002g0163 | 3 | HG02280.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+20188_-57+2020 others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39812646 | |||||
| chr6:39812663
|
C | G | 39 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0127others(36): Show | 39 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.-57+20198C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812663 | ||||||
| chr6:39812925
|
A | G | 1 | a0002c0010t0002g0256 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57+20460A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812925 | ||||||
| chr6:39812928
|
A | G | 83 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0065others(80): Show | 83 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-57+20463A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812928 | ||||||
| chr6:39813146
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0002g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-57+20688_-57+2070 others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39813146 | |||||
| chr6:39813166
|
G | A | 5 | a0001c0001t0001g0220a0001c0001t0001g0258a0001c0001t0008g0215others(2): Show | 5 | HG00323.hp2 HG00741.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+20701G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813166 | ||||||
| chr6:39813167
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+20702C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813167 | ||||||
| chr6:39813169
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+20704T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813169 | ||||||
| chr6:39813215
|
A | T | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57+20750A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813215 | ||||||
| chr6:39813537
|
C | A | 42 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0127others(39): Show | 42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+21072C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813537 | ||||||
| chr6:39813550
|
T | C | 2 | a0001c0001t0001g0234a0005c0023t0007g0233 | 2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-57+21085T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813550 | ||||||
| chr6:39813565
|
T | A | 42 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0127others(39): Show | 42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+21100T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813565 | ||||||
| chr6:39813578
|
CT | C | 14 | a0001c0001t0001g0235a0001c0001t0001g0272a0001c0001t0010g0269others(11): Show | 14 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+21114delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813578 | ||||||
| chr6:39813580
|
C | G | 1 | a0001c0007t0013g0246 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-57+21115C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813580 | ||||||
| chr6:39813708
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-57+21243C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813708 | ||||||
| chr6:39813728
|
C | T | 5 | a0001c0003t0016g0284a0001c0006t0020g0285a0001c0008t0005g0166others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+21263C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813728 | ||||||
| chr6:39813784
|
G | A | 120 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0065others(117): Show | 120 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.-57+21319G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813784 | ||||||
| chr6:39813927
|
A | C | 299 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.-57+21462A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813927 | ||||||
| chr6:39814016
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+21551C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814016 | ||||||
| chr6:39814058
|
C | T | 28 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00323.hp1 HG00621.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-57+21593C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814058 | ||||||
| chr6:39814083
|
C | G | 1 | a0001c0002t0002g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-57+21618C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814083 | ||||||
| chr6:39814188
|
C | CT | 8 | a0001c0001t0001g0112a0001c0001t0001g0208a0001c0005t0011g0042others(5): Show | 8 | HG01255.hp2 HG01361.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+21736dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39814188 | |||||
| chr6:39814188
|
CT | C | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.-57+21736delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39814188 | |||||
| chr6:39814191
|
T | TC | 92 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0065others(89): Show | 92 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-57+21726_-57+2172 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814191 | ||||||
| chr6:39814316
|
C | T | 190 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(187): Show | 190 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+21851C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814316 | ||||||
| chr6:39814455
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+21990G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814455 | ||||||
| chr6:39814461
|
G | A | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57+21996G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814461 | ||||||
| chr6:39814503
|
T | G | 162 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+22038T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814503 | ||||||
| chr6:39814580
|
A | G | 4 | a0001c0005t0011g0042a0001c0033t0001g0044a0001c0046t0001g0043others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+22115A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814580 | ||||||
| chr6:39814827
|
C | G | 2 | a0001c0003t0016g0206a0011c0029t0001g0177 | 2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-57+22362C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814827 | ||||||
| chr6:39814830
|
C | G | 4 | a0001c0005t0011g0042a0001c0033t0001g0044a0001c0046t0001g0043others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+22365C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814830 | ||||||
| chr6:39815083
|
A | C | 1 | a0001c0003t0003g0179 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-57+22618A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815083 | ||||||
| chr6:39815166
|
G | T | 1 | a0001c0009t0009g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57+22701G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815166 | ||||||
| chr6:39815372
|
A | G | 1 | a0014c0040t0002g0230 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-57+22907A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815372 | ||||||
| chr6:39815393
|
C | T | 4 | a0001c0005t0011g0042a0001c0033t0001g0044a0001c0046t0001g0043others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+22928C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815393 | ||||||
| chr6:39815439
|
C | A | 2 | a0001c0004t0003g0115a0001c0006t0001g0295 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-57+22974C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815439 | ||||||
| chr6:39815468
|
C | A | 162 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+23003C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815468 | ||||||
| chr6:39815498
|
C | T | 1 | a0002c0015t0003g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-57+23033C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815498 | ||||||
| chr6:39815542
|
A | G | 156 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(153): Show | 156 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.-57+23077A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815542 | ||||||
| chr6:39815582
|
G | T | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 204 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.-57+23117G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815582 | ||||||
| chr6:39815594
|
A | G | 9 | a0001c0001t0001g0189a0001c0001t0001g0198a0001c0001t0001g0201others(6): Show | 9 | HG00423.hp2 HG00609.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+23129A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815594 | ||||||
| chr6:39815620
|
C | T | 1 | a0001c0003t0003g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-57+23155C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815620 | ||||||
| chr6:39815651
|
T | TAC | 31 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0204others(28): Show | 31 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+23219_-57+2322 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
T | TACAC | 34 | a0001c0001t0001g0189a0001c0001t0001g0198a0001c0001t0001g0201others(31): Show | 34 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-57+23217_-57+2322 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
T | TACACAC | 14 | a0001c0001t0001g0034a0001c0001t0001g0151a0001c0001t0001g0235others(11): Show | 14 | HG00642.hp2 HG02083.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+23215_-57+2322 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
T | TACACACA others(1): Show |
12 | a0001c0001t0001g0112a0001c0001t0001g0131a0001c0001t0025g0031others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+23213_-57+2322 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
T | TACACACA others(3): Show |
7 | a0001c0001t0001g0182a0001c0002t0002g0020a0001c0002t0002g0023others(4): Show | 7 | HG02056.hp2 HG02135.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+23211_-57+2322 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
T | TACACACA others(5): Show |
2 | a0001c0003t0003g0270a0016c0043t0005g0150 | 2 | HG03225.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-57+23209_-57+2322 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
T | TACACACA others(7): Show |
1 | a0001c0002t0002g0019 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-57+23207_-57+2322 others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
T | TACACACA others(19): Show |
1 | a0001c0002t0002g0113 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+23195_-57+2322 others(30): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
TAC | T | 21 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0211others(18): Show | 21 | HG00741.hp1 HG01257.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-57+23219_-57+2322 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
TACACAC | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0164a0001c0002t0002g0107others(8): Show | 11 | HG00741.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+23215_-57+2322 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
TACACACA others(1): Show |
T | 144 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 144 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-57+23213_-57+2322 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
TACACACA others(3): Show |
T | 6 | a0001c0003t0016g0284a0001c0004t0006g0089a0001c0006t0020g0285others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+23211_-57+2322 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
TACACACA others(5): Show |
T | 1 | a0001c0006t0001g0013 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-57+23209_-57+2322 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815651
|
TACACACA others(9): Show |
T | 4 | a0001c0005t0011g0042a0001c0033t0001g0044a0001c0046t0001g0043others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+23205_-57+2322 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | |||||
| chr6:39815711
|
G | A | 2 | a0001c0001t0001g0234a0005c0023t0007g0233 | 2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-57+23246G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815711 | ||||||
| chr6:39815754
|
T | C | 1 | a0001c0003t0003g0260 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-57+23289T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815754 | ||||||
| chr6:39815853
|
A | C | 162 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+23388A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815853 | ||||||
| chr6:39815993
|
C | T | 162 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+23528C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815993 | ||||||
| chr6:39816056
|
C | T | 2 | a0001c0001t0001g0164a0001c0045t0002g0163 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+23591C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816056 | ||||||
| chr6:39816106
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-57+23641G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816106 | ||||||
| chr6:39816204
|
C | T | 11 | a0001c0001t0001g0235a0001c0001t0001g0272a0001c0001t0010g0269others(8): Show | 11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+23739C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816204 | ||||||
| chr6:39816358
|
T | C | 162 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+23893T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816358 | ||||||
| chr6:39816379
|
A | G | 2 | a0001c0005t0003g0292a0001c0005t0014g0175 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-57+23914A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816379 | ||||||
| chr6:39816413
|
G | T | 11 | a0001c0001t0001g0235a0001c0001t0001g0272a0001c0001t0010g0269others(8): Show | 11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+23948G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816413 | ||||||
| chr6:39816455
|
G | A | 1 | a0006c0021t0001g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-57+23990G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816455 | ||||||
| chr6:39816573
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-57+24108T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816573 | ||||||
| chr6:39816589
|
C | A | 180 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(177): Show | 180 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.-57+24124C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816589 | ||||||
| chr6:39816775
|
T | C | 1 | a0001c0008t0005g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-57+24310T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816775 | ||||||
| chr6:39816831
|
T | A | 1 | a0001c0002t0002g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-57+24366T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816831 | ||||||
| chr6:39816840
|
G | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.-57+24375G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816840 | ||||||
| chr6:39816857
|
C | T | 8 | a0001c0009t0009g0162a0001c0013t0023g0169a0001c0013t0023g0170others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+24392C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816857 | ||||||
| chr6:39816858
|
G | A | 2 | a0001c0008t0005g0166a0001c0036t0022g0167 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-57+24393G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816858 | ||||||
| chr6:39816927
|
A | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00323.hp1 HG00621.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-57+24462A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816927 | ||||||
| chr6:39816944
|
G | A | 162 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+24479G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816944 | ||||||
| chr6:39817422
|
G | A | 1 | a0001c0008t0005g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-57+24957G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817422 | ||||||
| chr6:39817595
|
G | A | 2 | a0001c0005t0003g0292a0001c0005t0014g0175 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-57+25130G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817595 | ||||||
| chr6:39817760
|
T | C | 1 | a0001c0001t0017g0267 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-57+25295T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817760 | ||||||
| chr6:39817783
|
C | G | 2 | a0001c0001t0001g0112a0017c0019t0003g0036 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-57+25318C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817783 | ||||||
| chr6:39817835
|
C | A | 1 | a0001c0006t0001g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+25370C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817835 | ||||||
| chr6:39817905
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG02647.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+25440A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817905 | ||||||
| chr6:39817944
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+25479C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817944 | ||||||
| chr6:39818051
|
C | T | 1 | a0001c0004t0031g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57+25586C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818051 | ||||||
| chr6:39818093
|
C | T | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57+25628C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818093 | ||||||
| chr6:39818127
|
C | T | 77 | a0001c0001t0001g0131a0001c0001t0001g0151a0001c0001t0001g0182others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.-57+25662C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818127 | ||||||
| chr6:39818136
|
G | A | 12 | a0001c0002t0030g0174a0001c0003t0003g0116a0001c0004t0021g0100others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+25671G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818136 | ||||||
| chr6:39818137
|
T | C | 178 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(175): Show | 178 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-57+25672T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818137 | ||||||
| chr6:39818138
|
C | A | 3 | a0001c0001t0001g0067a0001c0003t0039g0090a0018c0047t0001g0066 | 3 | HG02683.hp1 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-57+25673C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818138 | ||||||
| chr6:39818182
|
T | TA | 43 | a0001c0001t0001g0123a0001c0001t0001g0185a0001c0001t0001g0208others(40): Show | 43 | HG00621.hp1 HG01175.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.-57+25741dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39818182 | |||||
| chr6:39818182
|
T | TAA | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00621.hp2 HG01081.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-57+25740_-57+2574 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39818182 | |||||
| chr6:39818182
|
TA | T | 11 | a0001c0001t0001g0161a0001c0001t0001g0183a0001c0001t0001g0198others(8): Show | 11 | HG01169.hp2 HG01515.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+25741delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39818182 | |||||
| chr6:39818182
|
TAAAAAAA | T | 7 | a0001c0003t0016g0284a0001c0006t0020g0285a0001c0008t0005g0286others(4): Show | 7 | HG02055.hp2 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+25735_-57+2574 others(11): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39818182 | |||||
| chr6:39818200
|
A | AC | 13 | a0001c0002t0030g0174a0001c0003t0003g0116a0001c0004t0021g0100others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+25735_-57+2573 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818200 | ||||||
| chr6:39818204
|
A | AC | 86 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0065others(83): Show | 86 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-57+25739_-57+2574 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818204 | ||||||
| chr6:39818204
|
A | C | 1 | a0001c0002t0002g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-57+25739A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818204 | ||||||
| chr6:39818303
|
C | T | 3 | a0001c0002t0002g0276a0001c0006t0001g0032a0001c0012t0002g0298 | 3 | HG02486.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-57+25838C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818303 | ||||||
| chr6:39818317
|
A | G | 100 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0065others(97): Show | 100 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-57+25852A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818317 | ||||||
| chr6:39818351
|
C | A | 166 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 166 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-57+25886C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818351 | ||||||
| chr6:39818539
|
G | A | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+26074G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818539 | ||||||
| chr6:39818582
|
C | A | 13 | a0001c0001t0001g0118a0001c0001t0001g0185a0001c0001t0001g0198others(10): Show | 13 | HG00423.hp2 HG00621.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+26117C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818582 | ||||||
| chr6:39818643
|
G | A | 2 | a0001c0001t0001g0234a0005c0023t0007g0233 | 2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-57+26178G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818643 | ||||||
| chr6:39818867
|
T | C | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(217): Show | 220 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.-57+26402T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818867 | ||||||
| chr6:39819012
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-57+26547G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819012 | ||||||
| chr6:39819088
|
T | C | 252 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.-57+26623T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819088 | ||||||
| chr6:39819091
|
C | T | 2 | a0001c0001t0001g0118a0001c0004t0003g0102 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-57+26626C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819091 | ||||||
| chr6:39819242
|
G | A | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57+26777G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819242 | ||||||
| chr6:39819273
|
G | T | 7 | a0001c0001t0001g0164a0001c0001t0001g0227a0001c0001t0001g0273others(4): Show | 7 | HG02738.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+26808G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819273 | ||||||
| chr6:39819301
|
G | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+26836G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819301 | ||||||
| chr6:39819302
|
A | G | 5 | a0001c0005t0011g0124a0001c0005t0014g0175a0001c0009t0009g0111others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+26837A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819302 | ||||||
| chr6:39819408
|
A | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0118a0001c0001t0001g0281others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+26943A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819408 | ||||||
| chr6:39819529
|
G | A | 1 | a0001c0006t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-57+27064G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819529 | ||||||
| chr6:39819581
|
G | GA | 9 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0003t0003g0068others(6): Show | 9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+27123dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39819581 | |||||
| chr6:39819760
|
T | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+27295T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819760 | ||||||
| chr6:39819771
|
G | A | 13 | a0001c0001t0001g0123a0001c0001t0019g0050a0001c0002t0002g0180others(10): Show | 13 | HG00741.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+27306G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819771 | ||||||
| chr6:39819836
|
T | C | 13 | a0001c0001t0001g0123a0001c0001t0019g0050a0001c0002t0002g0180others(10): Show | 13 | HG00741.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+27371T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819836 | ||||||
| chr6:39819856
|
G | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+27391G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819856 | ||||||
| chr6:39819865
|
A | T | 3 | a0001c0002t0002g0133a0001c0005t0011g0030a0001c0009t0009g0128 | 3 | HG01109.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+27400A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819865 | ||||||
| chr6:39819903
|
C | T | 75 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(72): Show | 75 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-57+27438C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819903 | ||||||
| chr6:39819960
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-57+27495C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819960 | ||||||
| chr6:39819983
|
C | T | 16 | a0001c0001t0001g0208a0001c0001t0025g0031a0001c0002t0002g0276others(13): Show | 16 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+27518C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819983 | ||||||
| chr6:39820003
|
A | G | 19 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0123others(16): Show | 19 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-57+27538A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820003 | ||||||
| chr6:39820049
|
G | T | 2 | a0001c0002t0002g0184a0001c0003t0003g0268 | 2 | HG02135.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-57+27584G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820049 | ||||||
| chr6:39820112
|
T | C | 109 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(106): Show | 109 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.-57+27647T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820112 | ||||||
| chr6:39820231
|
C | T | 1 | a0002c0010t0002g0255 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-57+27766C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820231 | ||||||
| chr6:39820405
|
C | T | 1 | a0001c0009t0009g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57+27940C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820405 | ||||||
| chr6:39820522
|
C | T | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0003t0007g0016 | 3 | HG01175.hp1 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-57+28057C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820522 | ||||||
| chr6:39820582
|
G | T | 98 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(95): Show | 98 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-57+28117G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820582 | ||||||
| chr6:39820626
|
A | C | 9 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0003t0003g0068others(6): Show | 9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+28161A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820626 | ||||||
| chr6:39820720
|
A | G | 109 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(106): Show | 109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-57+28255A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820720 | ||||||
| chr6:39820753
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-57+28288A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820753 | ||||||
| chr6:39820825
|
G | A | 9 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0003t0003g0068others(6): Show | 9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+28360G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820825 | ||||||
| chr6:39820875
|
G | A | 1 | a0001c0003t0016g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-57+28410G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820875 | ||||||
| chr6:39820972
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | HG01891.hp2 HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-57+28507G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820972 | ||||||
| chr6:39821121
|
C | A | 2 | a0001c0004t0003g0115a0017c0019t0003g0036 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-57+28656C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821121 | ||||||
| chr6:39821175
|
GAGCCAC | G | 18 | a0001c0001t0001g0208a0001c0001t0025g0031a0001c0002t0002g0276others(15): Show | 18 | HG01081.hp1 HG01255.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+28712_-57+2871 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39821175 | |||||
| chr6:39821184
|
ATT | A | 18 | a0001c0001t0001g0208a0001c0001t0025g0031a0001c0002t0002g0276others(15): Show | 18 | HG01081.hp1 HG01255.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+28720_-57+2872 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821184 | ||||||
| chr6:39821220
|
G | C | 3 | a0001c0001t0001g0201a0001c0002t0002g0202a0001c0007t0013g0064 | 3 | NA18956.hp1 NA18993.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-57+28755G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821220 | ||||||
| chr6:39821268
|
A | G | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+28803A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821268 | ||||||
| chr6:39821290
|
G | A | 3 | a0001c0002t0002g0007a0001c0002t0002g0238a0001c0002t0002g0296 | 3 | NA18973.hp2 NA18982.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-57+28825G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821290 | ||||||
| chr6:39821421
|
G | A | 1 | a0002c0010t0002g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-57+28956G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821421 | ||||||
| chr6:39821620
|
G | T | 3 | a0001c0004t0021g0100a0001c0004t0035g0126a0001c0008t0005g0101 | 3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+29155G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821620 | ||||||
| chr6:39821794
|
C | G | 1 | a0001c0004t0006g0074 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-57+29329C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821794 | ||||||
| chr6:39821815
|
A | C | 48 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-57+29350A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821815 | ||||||
| chr6:39821955
|
G | A | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-57+29490G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821955 | ||||||
| chr6:39822085
|
G | C | 1 | a0001c0004t0004g0061 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-57+29620G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822085 | ||||||
| chr6:39822219
|
A | G | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+29754A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822219 | ||||||
| chr6:39822267
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0220a0001c0002t0002g0021 | 3 | HG01261.hp2 HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-57+29802C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822267 | ||||||
| chr6:39822411
|
C | T | 13 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0281others(10): Show | 13 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57+29946C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822411 | ||||||
| chr6:39822430
|
T | C | 12 | a0001c0002t0002g0038a0001c0002t0002g0278a0001c0004t0031g0294others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+29965T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822430 | ||||||
| chr6:39822434
|
G | A | 1 | a0001c0006t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-57+29969G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822434 | ||||||
| chr6:39822483
|
G | T | 1 | a0001c0002t0002g0140 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-57+30018G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822483 | ||||||
| chr6:39822527
|
A | C | 77 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(74): Show | 77 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-57+30062A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822527 | ||||||
| chr6:39822998
|
T | C | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+30533T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822998 | ||||||
| chr6:39823164
|
C | T | 97 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0076others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-57+30699C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823164 | ||||||
| chr6:39823269
|
T | C | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+30804T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823269 | ||||||
| chr6:39823307
|
C | A | 8 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0004t0004g0171others(5): Show | 8 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+30842C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823307 | ||||||
| chr6:39823519
|
C | G | 1 | a0001c0003t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-57+31054C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823519 | ||||||
| chr6:39823568
|
G | C | 2 | a0001c0044t0022g0114a0013c0038t0009g0041 | 2 | HG01361.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-57+31103G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823568 | ||||||
| chr6:39823574
|
C | T | 9 | a0001c0001t0001g0112a0001c0001t0019g0050a0001c0002t0002g0180others(6): Show | 9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+31109C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823574 | ||||||
| chr6:39823718
|
C | G | 1 | a0001c0032t0009g0168 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-57+31253C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823718 | ||||||
| chr6:39823781
|
G | A | 9 | a0001c0001t0001g0112a0001c0001t0019g0050a0001c0002t0002g0180others(6): Show | 9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+31316G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823781 | ||||||
| chr6:39823810
|
C | T | 10 | a0001c0001t0001g0071a0001c0001t0001g0160a0001c0001t0001g0258others(7): Show | 10 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57+31345C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823810 | ||||||
| chr6:39823883
|
C | A | 2 | a0001c0001t0001g0134a0001c0001t0008g0149 | 2 | HG01081.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-57+31418C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823883 | ||||||
| chr6:39823916
|
T | C | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+31451T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823916 | ||||||
| chr6:39823988
|
C | T | 97 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0076others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-57+31523C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823988 | ||||||
| chr6:39824119
|
G | A | 1 | a0012c0034t0001g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57+31654G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824119 | ||||||
| chr6:39824165
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+31700G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824165 | ||||||
| chr6:39824299
|
A | G | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+31834A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824299 | ||||||
| chr6:39824308
|
C | A | 3 | a0001c0001t0001g0118a0001c0005t0011g0030a0001c0009t0009g0128 | 3 | HG02970.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+31843C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824308 | ||||||
| chr6:39824476
|
G | A | 6 | a0001c0002t0002g0276a0001c0004t0003g0115a0001c0006t0028g0187others(3): Show | 6 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-31771G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824476 | ||||||
| chr6:39824503
|
T | A | 108 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(105): Show | 108 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-56-31744T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824503 | ||||||
| chr6:39824605
|
A | C | 1 | a0001c0002t0002g0045 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-56-31642A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824605 | ||||||
| chr6:39824737
|
T | C | 98 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0076others(95): Show | 98 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-56-31510T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824737 | ||||||
| chr6:39824755
|
G | A | 6 | a0001c0002t0002g0276a0001c0004t0003g0115a0001c0006t0028g0187others(3): Show | 6 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-31492G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824755 | ||||||
| chr6:39824769
|
G | A | 10 | a0001c0001t0001g0071a0001c0001t0001g0160a0001c0001t0001g0258others(7): Show | 10 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-31478G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824769 | ||||||
| chr6:39824981
|
G | A | 1 | a0001c0001t0017g0267 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-56-31266G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824981 | ||||||
| chr6:39825087
|
A | G | 25 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0001g0138others(22): Show | 25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-56-31160A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825087 | ||||||
| chr6:39825112
|
G | A | 9 | a0001c0001t0001g0208a0001c0001t0025g0031a0001c0003t0003g0176others(6): Show | 9 | HG01081.hp1 HG01255.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-31135G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825112 | ||||||
| chr6:39825156
|
A | C | 119 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(116): Show | 119 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-56-31091A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825156 | ||||||
| chr6:39825196
|
C | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-31051C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825196 | ||||||
| chr6:39825262
|
C | T | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-30985C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825262 | ||||||
| chr6:39825270
|
G | T | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-30977G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825270 | ||||||
| chr6:39825272
|
T | C | 12 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0281others(9): Show | 12 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-30975T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825272 | ||||||
| chr6:39825384
|
T | TAAAAC | 17 | a0001c0001t0001g0034a0001c0001t0017g0267a0001c0001t0019g0121others(14): Show | 17 | HG01978.hp1 HG02280.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.-56-30821_-56-3081 others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | |||||
| chr6:39825384
|
T | TAAAACAA others(3): Show |
2 | a0001c0003t0016g0122a0003c0024t0001g0028 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-56-30826_-56-3081 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | |||||
| chr6:39825384
|
TAAAAC | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 107 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-56-30821_-56-3081 others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | |||||
| chr6:39825384
|
TAAAACAA others(3): Show |
T | 8 | a0001c0001t0001g0131a0001c0001t0001g0151a0001c0001t0010g0269others(5): Show | 8 | HG01361.hp2 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-30826_-56-3081 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | |||||
| chr6:39825384
|
TAAAACAA others(8): Show |
T | 12 | a0001c0001t0001g0039a0001c0001t0001g0281a0001c0001t0001g0282others(9): Show | 12 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-30831_-56-3081 others(19): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | |||||
| chr6:39825384
|
TAAAACAA others(13): Show |
T | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-56-30836_-56-3081 others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | |||||
| chr6:39825443
|
GT | G | 20 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0019g0050others(17): Show | 20 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-56-30802delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825443 | |||||
| chr6:39825444
|
T | TG | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0088others(38): Show | 41 | HG00609.hp1 HG00741.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.-56-30803_-56-3080 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825444 | ||||||
| chr6:39825444
|
T | TGGG | 3 | a0001c0001t0001g0123a0001c0004t0021g0060a0001c0009t0009g0162 | 3 | HG02055.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-30803_-56-3080 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825444 | ||||||
| chr6:39825445
|
T | G | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-56-30802T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825445 | ||||||
| chr6:39825447
|
GT | G | 9 | a0001c0002t0002g0278a0001c0004t0031g0294a0001c0005t0011g0042others(6): Show | 9 | HG02280.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-30799delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825447 | ||||||
| chr6:39825448
|
T | G | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-56-30799T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825448 | ||||||
| chr6:39825452
|
G | T | 4 | a0001c0001t0001g0112a0001c0003t0016g0206a0001c0036t0022g0167others(1): Show | 4 | HG02818.hp2 HG02886.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-30795G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825452 | ||||||
| chr6:39825453
|
G | T | 3 | a0001c0003t0016g0206a0001c0036t0022g0167a0011c0029t0001g0177 | 3 | HG02818.hp2 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-56-30794G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825453 | ||||||
| chr6:39825455
|
C | G | 48 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-56-30792C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825455 | ||||||
| chr6:39825534
|
G | A | 50 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-56-30713G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825534 | ||||||
| chr6:39825552
|
C | T | 5 | a0001c0001t0001g0123a0001c0003t0003g0116a0001c0004t0021g0060others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-30695C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825552 | ||||||
| chr6:39825557
|
C | A | 3 | a0001c0001t0025g0031a0001c0022t0020g0047a0016c0043t0005g0150 | 3 | HG03225.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-56-30690C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825557 | ||||||
| chr6:39825670
|
G | C | 9 | a0001c0001t0001g0034a0001c0002t0002g0113a0001c0002t0002g0191others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-30577G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825670 | ||||||
| chr6:39825704
|
T | C | 76 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-56-30543T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825704 | ||||||
| chr6:39825754
|
G | C | 1 | a0001c0002t0002g0283 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-56-30493G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825754 | ||||||
| chr6:39825948
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-56-30299A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825948 | ||||||
| chr6:39826155
|
C | T | 4 | a0001c0003t0003g0287a0001c0003t0003g0289a0001c0003t0003g0290others(1): Show | 4 | HG02083.hp1 HG02523.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-30092C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39826155 | ||||||
| chr6:39826264
|
A | AT | 92 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0075others(89): Show | 92 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-56-29973dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39826264 | |||||
| chr6:39826483
|
C | G | 1 | a0001c0002t0002g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-56-29764C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39826483 | ||||||
| chr6:39826582
|
C | T | 8 | a0001c0001t0001g0112a0001c0001t0019g0050a0001c0002t0002g0180others(5): Show | 8 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-29665C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39826582 | ||||||
| chr6:39826877
|
A | G | 107 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(104): Show | 107 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-56-29370A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39826877 | ||||||
| chr6:39827030
|
C | G | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 118 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-29217C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827030 | ||||||
| chr6:39827142
|
G | A | 1 | a0001c0006t0020g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-56-29105G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827142 | ||||||
| chr6:39827238
|
C | T | 1 | a0001c0003t0003g0099 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-56-29009C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827238 | ||||||
| chr6:39827263
|
G | GC | 107 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(104): Show | 107 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-56-28984_-56-2898 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827263 | ||||||
| chr6:39827313
|
G | A | 7 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0004t0004g0171others(4): Show | 7 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-28934G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827313 | ||||||
| chr6:39827345
|
G | A | 11 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0281others(8): Show | 11 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-28902G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827345 | ||||||
| chr6:39827424
|
A | G | 16 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0123others(13): Show | 16 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-28823A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827424 | ||||||
| chr6:39827455
|
G | A | 7 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0004t0004g0171others(4): Show | 7 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-28792G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827455 | ||||||
| chr6:39827469
|
T | C | 16 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0123others(13): Show | 16 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-28778T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827469 | ||||||
| chr6:39827513
|
C | T | 16 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0123others(13): Show | 16 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-28734C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827513 | ||||||
| chr6:39827558
|
G | A | 1 | a0001c0004t0004g0061 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-56-28689G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827558 | ||||||
| chr6:39827564
|
G | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0220a0001c0002t0002g0021 | 3 | HG01261.hp2 HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-56-28683G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827564 | ||||||
| chr6:39827577
|
C | T | 1 | a0001c0002t0002g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-56-28670C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827577 | ||||||
| chr6:39827652
|
T | C | 18 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0123others(15): Show | 18 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-56-28595T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827652 | ||||||
| chr6:39827773
|
C | T | 80 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-56-28474C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827773 | ||||||
| chr6:39827774
|
A | G | 258 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.-56-28473A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827774 | ||||||
| chr6:39827829
|
G | C | 97 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0076others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-56-28418G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827829 | ||||||
| chr6:39827844
|
T | TCTC | 127 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(124): Show | 127 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-56-28401_-56-2840 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39827844 | |||||
| chr6:39827938
|
C | T | 1 | a0001c0002t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-56-28309C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827938 | ||||||
| chr6:39828017
|
G | A | 28 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0137others(25): Show | 28 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-56-28230G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828017 | ||||||
| chr6:39828112
|
G | A | 1 | a0001c0006t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-28135G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828112 | ||||||
| chr6:39828221
|
C | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-28026C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828221 | ||||||
| chr6:39828226
|
A | G | 76 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-56-28021A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828226 | ||||||
| chr6:39828556
|
C | T | 7 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0004t0004g0171others(4): Show | 7 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-27691C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828556 | ||||||
| chr6:39828559
|
C | G | 96 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0076others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-56-27688C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828559 | ||||||
| chr6:39828567
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0123a0001c0003t0003g0116 | 3 | HG03098.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-56-27680C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828567 | ||||||
| chr6:39828570
|
C | CTTTTTTT others(3): Show |
30 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0001g0138others(27): Show | 30 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-56-27675_-56-2766 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | |||||
| chr6:39828570
|
C | CTTTTTTT others(4): Show |
19 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(16): Show | 19 | HG00741.hp2 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-56-27676_-56-2766 others(15): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | |||||
| chr6:39828570
|
C | CTTTTTTT others(5): Show |
35 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0109others(32): Show | 35 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.-56-27666_-56-2766 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | |||||
| chr6:39828570
|
C | CTTTTTTT others(6): Show |
7 | a0001c0001t0001g0281a0001c0002t0002g0184a0001c0002t0002g0202others(4): Show | 7 | HG02055.hp1 HG03927.hp2 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-27666_-56-2766 others(17): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | |||||
| chr6:39828570
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0039a0001c0001t0001g0123a0001c0001t0001g0282 | 3 | HG01891.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-56-27666_-56-2766 others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | |||||
| chr6:39828587
|
G | A | 5 | a0001c0001t0019g0050a0001c0006t0001g0158a0001c0008t0005g0166others(2): Show | 5 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-27660G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828587 | ||||||
| chr6:39828665
|
T | C | 9 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0004t0004g0171others(6): Show | 9 | HG00741.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-27582T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828665 | ||||||
| chr6:39828688
|
G | A | 89 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0076others(86): Show | 89 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-56-27559G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828688 | ||||||
| chr6:39828710
|
G | A | 4 | a0001c0003t0003g0002a0001c0003t0003g0035a0001c0003t0003g0257others(1): Show | 4 | HG01943.hp2 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-27537G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828710 | ||||||
| chr6:39828723
|
C | T | 7 | a0001c0001t0019g0050a0001c0002t0002g0180a0001c0004t0004g0171others(4): Show | 7 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-27524C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828723 | ||||||
| chr6:39828724
|
G | A | 9 | a0001c0001t0001g0160a0001c0001t0019g0121a0001c0003t0007g0001others(6): Show | 9 | HG01074.hp1 HG01109.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-27523G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828724 | ||||||
| chr6:39828768
|
G | T | 79 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(76): Show | 79 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-56-27479G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828768 | ||||||
| chr6:39828808
|
G | A | 2 | a0001c0001t0001g0155a0001c0002t0002g0120 | 2 | HG01261.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-56-27439G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828808 | ||||||
| chr6:39828891
|
C | T | 28 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0137others(25): Show | 28 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-56-27356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828891 | ||||||
| chr6:39828895
|
C | T | 17 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0123others(14): Show | 17 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-56-27352C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828895 | ||||||
| chr6:39828896
|
C | G | 2 | a0001c0004t0021g0060a0001c0009t0009g0162 | 2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-27351C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828896 | ||||||
| chr6:39828908
|
G | A | 136 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(133): Show | 136 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-56-27339G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828908 | ||||||
| chr6:39828933
|
T | C | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-27314T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828933 | ||||||
| chr6:39829064
|
C | G | 9 | a0001c0001t0001g0208a0001c0001t0025g0031a0001c0003t0003g0176others(6): Show | 9 | HG01081.hp1 HG01255.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-27183C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829064 | ||||||
| chr6:39829134
|
C | T | 48 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-56-27113C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829134 | ||||||
| chr6:39829167
|
C | T | 26 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0137others(23): Show | 26 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.-56-27080C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829167 | ||||||
| chr6:39829176
|
T | C | 96 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0076others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-56-27071T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829176 | ||||||
| chr6:39829374
|
C | T | 1 | a0001c0002t0002g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-56-26873C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829374 | ||||||
| chr6:39829420
|
C | T | 2 | a0001c0003t0003g0290a0010c0028t0004g0291 | 2 | NA18747.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-56-26827C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829420 | ||||||
| chr6:39829503
|
G | C | 1 | a0001c0031t0040g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-56-26744G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829503 | ||||||
| chr6:39829608
|
T | C | 76 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-56-26639T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829608 | ||||||
| chr6:39830076
|
G | T | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-56-26171G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830076 | ||||||
| chr6:39830181
|
C | T | 11 | a0001c0001t0001g0160a0001c0001t0001g0258a0001c0001t0001g0259others(8): Show | 11 | HG01074.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-26066C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830181 | ||||||
| chr6:39830396
|
C | T | 19 | a0001c0001t0001g0208a0001c0001t0025g0031a0001c0002t0002g0276others(16): Show | 19 | HG01081.hp1 HG01255.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.-56-25851C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830396 | ||||||
| chr6:39830463
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-56-25784C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830463 | ||||||
| chr6:39830485
|
G | A | 1 | a0002c0015t0003g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-56-25762G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830485 | ||||||
| chr6:39830505
|
G | C | 1 | a0001c0006t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-56-25742G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830505 | ||||||
| chr6:39830547
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-56-25700C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830547 | ||||||
| chr6:39830549
|
G | A | 10 | a0001c0001t0001g0118a0001c0002t0002g0278a0001c0004t0031g0294others(7): Show | 10 | HG02280.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-25698G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830549 | ||||||
| chr6:39830581
|
A | C | 106 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(103): Show | 106 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-56-25666A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830581 | ||||||
| chr6:39830668
|
C | T | 1 | a0001c0004t0006g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-56-25579C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830668 | ||||||
| chr6:39830669
|
G | A | 1 | a0001c0006t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-25578G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830669 | ||||||
| chr6:39830690
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-56-25557C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830690 | ||||||
| chr6:39830695
|
A | T | 6 | a0001c0001t0001g0112a0001c0001t0001g0123a0001c0003t0003g0116others(3): Show | 6 | HG02055.hp1 HG02486.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-25552A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830695 | ||||||
| chr6:39830702
|
A | G | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-25545A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830702 | ||||||
| chr6:39830784
|
T | C | 2 | a0001c0006t0001g0040a0001c0008t0005g0025 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-56-25463T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830784 | ||||||
| chr6:39830892
|
C | T | 1 | a0001c0003t0016g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-25355C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830892 | ||||||
| chr6:39830933
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0273 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-56-25314C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830933 | ||||||
| chr6:39830935
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-56-25312A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830935 | ||||||
| chr6:39830986
|
A | G | 2 | a0001c0001t0001g0123a0001c0003t0003g0116 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-25261A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830986 | ||||||
| chr6:39831083
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-56-25164A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831083 | ||||||
| chr6:39831137
|
G | T | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-56-25110G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831137 | ||||||
| chr6:39831240
|
G | A | 2 | a0001c0002t0002g0019a0001c0002t0002g0020 | 2 | NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-56-25007G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831240 | ||||||
| chr6:39831364
|
C | T | 2 | a0001c0004t0021g0060a0001c0009t0009g0162 | 2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-24883C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831364 | ||||||
| chr6:39831416
|
T | C | 5 | a0001c0001t0001g0039a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-24831T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831416 | ||||||
| chr6:39831551
|
TCTAGGAT others(5): Show |
T | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-56-24694_-56-2468 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831551 | |||||
| chr6:39831696
|
TG | T | 80 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(77): Show | 80 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-56-24545delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831696 | |||||
| chr6:39831697
|
G | T | 3 | a0001c0001t0001g0137a0001c0002t0002g0254a0001c0003t0003g0035 | 3 | HG01257.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-56-24550G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831697 | ||||||
| chr6:39831735
|
C | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-24512C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831735 | ||||||
| chr6:39831738
|
G | A | 2 | a0001c0001t0001g0262a0001c0002t0002g0261 | 2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-56-24509G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831738 | ||||||
| chr6:39831780
|
A | AGGGGGCA others(9): Show |
1 | a0001c0004t0021g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-56-24461_-56-2444 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831780 | |||||
| chr6:39831792
|
C | T | 2 | a0001c0001t0001g0123a0001c0008t0005g0101 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-56-24455C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831792 | ||||||
| chr6:39831796
|
G | GGGGGGCA others(93): Show |
1 | a0001c0001t0001g0208 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-56-24446_-56-2444 others(104): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831796 | |||||
| chr6:39831798
|
G | GGGGCAGG others(8): Show |
98 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(95): Show | 98 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-56-24446_-56-2444 others(19): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831798 | |||||
| chr6:39831834
|
G | GGGGTAGG others(111): Show |
1 | a0001c0001t0001g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-24356_-56-2435 others(122): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831834 | |||||
| chr6:39831892
|
G | A | 49 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-56-24355G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831892 | ||||||
| chr6:39831892
|
G | GTGCACTG others(111): Show |
1 | a0001c0004t0026g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-56-24331_-56-2433 others(122): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831892 | |||||
| chr6:39831928
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-56-24319C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831928 | ||||||
| chr6:39831938
|
G | GA | 99 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0071others(96): Show | 99 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-56-24309_-56-2430 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831938 | ||||||
| chr6:39832053
|
G | A | 1 | a0001c0003t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-24194G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832053 | ||||||
| chr6:39832113
|
C | T | 1 | a0001c0003t0003g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-56-24134C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832113 | ||||||
| chr6:39832197
|
A | C | 4 | a0001c0001t0001g0211a0001c0001t0001g0265a0001c0002t0002g0264others(1): Show | 4 | HG00735.hp2 HG01952.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-24050A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832197 | ||||||
| chr6:39832238
|
A | G | 85 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(82): Show | 85 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-56-24009A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832238 | ||||||
| chr6:39832399
|
C | T | 52 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-56-23848C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832399 | ||||||
| chr6:39832436
|
AT | A | 52 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-56-23809delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39832436 | |||||
| chr6:39832489
|
C | T | 1 | a0001c0002t0002g0296 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-56-23758C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832489 | ||||||
| chr6:39832584
|
T | C | 52 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-56-23663T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832584 | ||||||
| chr6:39832591
|
GTC | G | 51 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0086others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-56-23652_-56-2365 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39832591 | |||||
| chr6:39832606
|
G | A | 1 | a0001c0008t0005g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-23641G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832606 | ||||||
| chr6:39832662
|
G | C | 1 | a0001c0006t0001g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-56-23585G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832662 | ||||||
| chr6:39832693
|
CTTCCTGG others(15): Show |
C | 1 | a0001c0001t0001g0164 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-56-23546_-56-2352 others(26): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39832693 | |||||
| chr6:39832762
|
T | A | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-23485T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832762 | ||||||
| chr6:39832770
|
G | A | 1 | a0001c0009t0009g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-56-23477G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832770 | ||||||
| chr6:39832801
|
G | A | 38 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0137others(35): Show | 38 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.-56-23446G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832801 | ||||||
| chr6:39832835
|
C | G | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-23412C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832835 | ||||||
| chr6:39832846
|
C | T | 10 | a0001c0001t0001g0034a0001c0002t0002g0113a0001c0002t0002g0191others(7): Show | 10 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-23401C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832846 | ||||||
| chr6:39832854
|
T | C | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-23393T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832854 | ||||||
| chr6:39832881
|
C | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-23366C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832881 | ||||||
| chr6:39832893
|
T | G | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-23354T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832893 | ||||||
| chr6:39832934
|
C | G | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-23313C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832934 | ||||||
| chr6:39832996
|
G | A | 7 | a0001c0001t0001g0203a0001c0001t0001g0248a0001c0002t0002g0186others(4): Show | 7 | HG00621.hp2 NA18747.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-23251G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832996 | ||||||
| chr6:39833052
|
G | A | 1 | a0001c0007t0012g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-56-23195G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833052 | ||||||
| chr6:39833061
|
C | T | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-23186C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833061 | ||||||
| chr6:39833198
|
G | A | 36 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0137others(33): Show | 36 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.-56-23049G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833198 | ||||||
| chr6:39833270
|
C | G | 7 | a0001c0001t0001g0112a0001c0002t0002g0133a0001c0004t0021g0100others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-22977C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833270 | ||||||
| chr6:39833458
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-56-22789C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833458 | ||||||
| chr6:39833527
|
C | T | 1 | a0001c0006t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-22720C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833527 | ||||||
| chr6:39833561
|
G | C | 3 | a0001c0004t0021g0100a0001c0004t0035g0126a0001c0008t0005g0101 | 3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-22686G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833561 | ||||||
| chr6:39833725
|
A | G | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-22522A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833725 | ||||||
| chr6:39833839
|
A | G | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-22408A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833839 | ||||||
| chr6:39833944
|
A | G | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-22303A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833944 | ||||||
| chr6:39834083
|
G | A | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-22164G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834083 | ||||||
| chr6:39834428
|
G | C | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-21819G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834428 | ||||||
| chr6:39834428
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-56-21819G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834428 | ||||||
| chr6:39834459
|
G | A | 3 | a0001c0004t0021g0100a0001c0004t0035g0126a0001c0008t0005g0101 | 3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-21788G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834459 | ||||||
| chr6:39834548
|
G | A | 1 | a0001c0006t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-21699G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834548 | ||||||
| chr6:39834813
|
C | A | 65 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-56-21434C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834813 | ||||||
| chr6:39834833
|
A | G | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-21414A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834833 | ||||||
| chr6:39834878
|
C | T | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-21369C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834878 | ||||||
| chr6:39835005
|
C | T | 1 | a0001c0002t0002g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-21242C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835005 | ||||||
| chr6:39835032
|
C | T | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-21215C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835032 | ||||||
| chr6:39835039
|
C | T | 12 | a0001c0001t0001g0034a0001c0002t0002g0113a0001c0002t0002g0191others(9): Show | 12 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-21208C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835039 | ||||||
| chr6:39835090
|
T | C | 71 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(68): Show | 71 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-56-21157T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835090 | ||||||
| chr6:39835148
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-56-21099C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835148 | ||||||
| chr6:39835224
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-56-21023C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835224 | ||||||
| chr6:39835352
|
A | G | 1 | a0001c0001t0010g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56-20895A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835352 | ||||||
| chr6:39835411
|
C | T | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-20836C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835411 | ||||||
| chr6:39835688
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-56-20559G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835688 | ||||||
| chr6:39835692
|
C | T | 1 | a0001c0004t0021g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-56-20555C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835692 | ||||||
| chr6:39835714
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-56-20533G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835714 | ||||||
| chr6:39835752
|
G | A | 4 | a0001c0007t0003g0058a0001c0007t0013g0207a0001c0007t0015g0057others(1): Show | 4 | NA18945.hp1 NA18960.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-20495G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835752 | ||||||
| chr6:39835773
|
C | A | 1 | a0001c0006t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-20474C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835773 | ||||||
| chr6:39835891
|
G | T | 1 | a0001c0006t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-20356G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835891 | ||||||
| chr6:39836349
|
G | A | 76 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-56-19898G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836349 | ||||||
| chr6:39836373
|
C | T | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-19874C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836373 | ||||||
| chr6:39836375
|
A | G | 74 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-19872A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836375 | ||||||
| chr6:39836404
|
G | A | 1 | a0001c0012t0002g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-56-19843G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836404 | ||||||
| chr6:39836451
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-56-19796A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836451 | ||||||
| chr6:39836476
|
TGAA | T | 3 | a0001c0001t0001g0153a0001c0001t0008g0148a0001c0002t0002g0133 | 3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-19768_-56-1976 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39836476 | |||||
| chr6:39836558
|
A | G | 1 | a0001c0003t0016g0284 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-56-19689A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836558 | ||||||
| chr6:39836616
|
C | T | 1 | a0013c0038t0009g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-56-19631C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836616 | ||||||
| chr6:39836618
|
C | G | 2 | a0001c0005t0011g0030a0001c0009t0009g0128 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-19629C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836618 | ||||||
| chr6:39836684
|
A | G | 1 | a0001c0006t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-19563A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836684 | ||||||
| chr6:39836728
|
C | T | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-19519C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836728 | ||||||
| chr6:39836881
|
T | C | 1 | a0001c0001t0019g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-56-19366T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836881 | ||||||
| chr6:39837087
|
A | G | 76 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-56-19160A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837087 | ||||||
| chr6:39837094
|
G | A | 1 | a0001c0003t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-19153G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837094 | ||||||
| chr6:39837203
|
A | G | 74 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-19044A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837203 | ||||||
| chr6:39837214
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-19033C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837214 | ||||||
| chr6:39837215
|
G | A | 73 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(70): Show | 73 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-56-19032G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837215 | ||||||
| chr6:39837233
|
A | T | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-19014A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837233 | ||||||
| chr6:39837245
|
G | C | 2 | a0001c0005t0003g0292a0001c0006t0020g0285 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-19002G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837245 | ||||||
| chr6:39837335
|
G | C | 76 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-56-18912G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837335 | ||||||
| chr6:39837339
|
T | C | 74 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-18908T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837339 | ||||||
| chr6:39837409
|
A | G | 5 | a0001c0001t0001g0242a0001c0001t0032g0243a0001c0016t0004g0054others(2): Show | 5 | NA18963.hp2 NA18994.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-18838A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837409 | ||||||
| chr6:39837417
|
T | C | 12 | a0001c0001t0001g0034a0001c0002t0002g0113a0001c0002t0002g0191others(9): Show | 12 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-18830T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837417 | ||||||
| chr6:39837446
|
T | C | 76 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-56-18801T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837446 | ||||||
| chr6:39837492
|
G | A | 3 | a0001c0004t0021g0100a0001c0004t0035g0126a0001c0008t0005g0101 | 3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-18755G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837492 | ||||||
| chr6:39837607
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0281others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-18640G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837607 | ||||||
| chr6:39837650
|
C | G | 63 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-56-18597C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837650 | ||||||
| chr6:39837663
|
C | CA | 39 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0001g0127others(36): Show | 39 | HG00741.hp2 HG01169.hp2 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.-56-18561dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837663
|
C | CAAAAA | 9 | a0001c0001t0001g0123a0001c0003t0016g0206a0001c0004t0004g0139others(6): Show | 9 | HG01081.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-18565_-56-1856 others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837663
|
C | CAAAAAA | 39 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0109others(36): Show | 39 | HG00438.hp1 HG00609.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.-56-18566_-56-1856 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837663
|
C | CAAAAAAA | 14 | a0001c0001t0001g0034a0001c0001t0001g0182a0001c0002t0002g0184others(11): Show | 14 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-18567_-56-1856 others(11): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837663
|
C | CAAAAAAA others(5): Show |
2 | a0001c0004t0021g0100a0001c0008t0005g0101 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-56-18572_-56-1856 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837663
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0017g0267 | 3 | HG01891.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-56-18575_-56-1856 others(19): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837663
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-56-18576_-56-1856 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837663
|
C | CAAAAAAA others(10): Show |
1 | a0001c0003t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-18577_-56-1856 others(21): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837663
|
CA | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0231a0001c0002t0002g0202others(7): Show | 10 | HG01975.hp2 HG02040.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-18561delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | |||||
| chr6:39837679
|
A | G | 1 | a0001c0001t0010g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56-18568A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837679 | ||||||
| chr6:39837687
|
G | A | 2 | a0001c0001t0001g0274a0001c0012t0002g0241 | 2 | NA19011.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-56-18560G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837687 | ||||||
| chr6:39837692
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-56-18555G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837692 | ||||||
| chr6:39838029
|
C | T | 2 | a0001c0005t0003g0292a0001c0006t0020g0285 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-18218C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838029 | ||||||
| chr6:39838446
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-17801C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838446 | ||||||
| chr6:39838497
|
C | T | 61 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-56-17750C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838497 | ||||||
| chr6:39838649
|
C | T | 36 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0137others(33): Show | 36 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.-56-17598C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838649 | ||||||
| chr6:39838799
|
C | T | 1 | a0001c0002t0002g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-56-17448C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838799 | ||||||
| chr6:39838891
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-56-17356G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838891 | ||||||
| chr6:39838891
|
G | T | 78 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(75): Show | 78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-56-17356G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838891 | ||||||
| chr6:39838899
|
C | T | 78 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(75): Show | 78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-56-17348C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838899 | ||||||
| chr6:39838902
|
A | AC | 3 | a0001c0001t0001g0153a0001c0001t0008g0148a0001c0002t0002g0133 | 3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-17342dupC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39838902 | |||||
| chr6:39838963
|
CT | C | 63 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-56-17281delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39838963 | |||||
| chr6:39838983
|
G | T | 3 | a0001c0001t0010g0084a0001c0003t0003g0059a0002c0015t0003g0217 | 3 | HG00423.hp1 HG02129.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-56-17264G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838983 | ||||||
| chr6:39839031
|
T | C | 74 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-17216T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839031 | ||||||
| chr6:39839032
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0008g0148a0001c0002t0002g0133 | 3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-17215C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839032 | ||||||
| chr6:39839059
|
A | G | 2 | a0001c0005t0003g0292a0001c0006t0020g0285 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-17188A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839059 | ||||||
| chr6:39839089
|
T | C | 230 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-56-17158T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839089 | ||||||
| chr6:39839090
|
G | A | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-17157G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839090 | ||||||
| chr6:39839090
|
G | GT | 6 | a0001c0001t0001g0093a0001c0001t0001g0213a0001c0002t0002g0097others(3): Show | 6 | HG02055.hp1 HG02738.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-17147dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39839090 | |||||
| chr6:39839224
|
T | C | 1 | a0001c0003t0003g0196 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-56-17023T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839224 | ||||||
| chr6:39839251
|
C | T | 2 | a0001c0005t0003g0292a0001c0006t0020g0285 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-16996C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839251 | ||||||
| chr6:39839312
|
G | C | 74 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-16935G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839312 | ||||||
| chr6:39839319
|
T | A | 63 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-56-16928T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839319 | ||||||
| chr6:39839515
|
G | A | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-56-16732G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839515 | ||||||
| chr6:39839562
|
T | G | 2 | a0001c0005t0003g0292a0001c0006t0020g0285 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-16685T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839562 | ||||||
| chr6:39839716
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0008g0148a0001c0002t0002g0133 | 3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-16531C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839716 | ||||||
| chr6:39839938
|
G | T | 70 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(67): Show | 70 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-56-16309G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839938 | ||||||
| chr6:39840048
|
G | A | 1 | a0001c0003t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-16199G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840048 | ||||||
| chr6:39840054
|
C | T | 12 | a0001c0001t0001g0034a0001c0002t0002g0113a0001c0002t0002g0191others(9): Show | 12 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-16193C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840054 | ||||||
| chr6:39840104
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0008g0148a0001c0002t0002g0133 | 3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-16143A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840104 | ||||||
| chr6:39840119
|
C | T | 74 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0075others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-16128C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840119 | ||||||
| chr6:39840142
|
G | A | 59 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(56): Show | 59 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.-56-16105G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840142 | ||||||
| chr6:39840184
|
A | G | 10 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-16063A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840184 | ||||||
| chr6:39840229
|
A | AAAAC | 10 | a0001c0001t0001g0039a0001c0001t0001g0153a0001c0001t0001g0281others(7): Show | 10 | HG01109.hp1 HG01169.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-15996_-56-1599 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39840229 | |||||
| chr6:39840229
|
A | AAAACAAA others(1): Show |
3 | a0001c0001t0001g0112a0001c0005t0011g0030a0001c0009t0009g0128 | 3 | HG03195.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-56-16000_-56-1599 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39840229 | |||||
| chr6:39840277
|
T | C | 1 | a0005c0023t0007g0233 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-56-15970T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840277 | ||||||
| chr6:39840288
|
C | A | 3 | a0001c0004t0021g0100a0001c0004t0035g0126a0001c0008t0005g0101 | 3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-15959C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840288 | ||||||
| chr6:39840324
|
G | A | 1 | a0001c0006t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-15923G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840324 | ||||||
| chr6:39840380
|
C | T | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-15867C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840380 | ||||||
| chr6:39840487
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0194 | 2 | HG00642.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-56-15760C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840487 | ||||||
| chr6:39840771
|
G | A | 26 | a0001c0001t0001g0072a0001c0001t0001g0093a0001c0001t0001g0183others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.-56-15476G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840771 | ||||||
| chr6:39840908
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-56-15339G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840908 | ||||||
| chr6:39840928
|
A | G | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-15319A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840928 | ||||||
| chr6:39841045
|
GGCAGGGT others(173): Show |
G | 3 | a0001c0001t0001g0096a0001c0002t0002g0097a0001c0003t0003g0008 | 3 | HG02004.hp2 NA19006.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-56-15161_-56-1498 others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39841045 | |||||
| chr6:39841086
|
AGGGGGAG others(173): Show |
A | 67 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-56-15042_-56-1486 others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39841086 | |||||
| chr6:39841236
|
A | G | 1 | a0001c0009t0009g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-56-15011A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841236 | ||||||
| chr6:39841242
|
A | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0001g0259others(5): Show | 8 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-15005A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841242 | ||||||
| chr6:39841248
|
G | T | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-14999G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841248 | ||||||
| chr6:39841255
|
A | G | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-14992A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841255 | ||||||
| chr6:39841261
|
G | A | 1 | a0001c0003t0007g0001 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-56-14986G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841261 | ||||||
| chr6:39841263
|
TCCGGGGG others(97): Show |
T | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-14981_-56-1487 others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39841263 | |||||
| chr6:39841266
|
G | A | 13 | a0001c0001t0001g0039a0001c0001t0001g0112a0001c0001t0001g0153others(10): Show | 13 | HG01109.hp1 HG01169.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-14981G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841266 | ||||||
| chr6:39841378
|
G | C | 58 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-56-14869G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841378 | ||||||
| chr6:39841390
|
G | C | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-14857G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841390 | ||||||
| chr6:39841420
|
G | A | 1 | a0001c0002t0002g0283 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-56-14827G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841420 | ||||||
| chr6:39841430
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0008g0148a0001c0002t0002g0133 | 3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-14817G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841430 | ||||||
| chr6:39841480
|
G | T | 2 | a0001c0003t0003g0116a0001c0006t0001g0152 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-14767G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841480 | ||||||
| chr6:39841484
|
C | T | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(85): Show | 88 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-56-14763C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841484 | ||||||
| chr6:39841541
|
T | C | 1 | a0001c0002t0002g0283 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-56-14706T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841541 | ||||||
| chr6:39841859
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-56-14388C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841859 | ||||||
| chr6:39841891
|
C | T | 1 | a0001c0009t0009g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-56-14356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841891 | ||||||
| chr6:39842170
|
G | T | 1 | a0001c0003t0003g0099 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-56-14077G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842170 | ||||||
| chr6:39842234
|
AAGAGCTC others(4): Show |
A | 1 | a0004c0020t0001g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-14010_-56-1400 others(15): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39842234 | |||||
| chr6:39842251
|
T | G | 1 | a0014c0040t0002g0230 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-56-13996T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842251 | ||||||
| chr6:39842271
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-56-13976T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842271 | ||||||
| chr6:39842279
|
G | A | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-13968G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842279 | ||||||
| chr6:39842372
|
G | A | 1 | a0001c0008t0005g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-56-13875G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842372 | ||||||
| chr6:39842463
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-56-13784C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842463 | ||||||
| chr6:39842489
|
C | T | 2 | a0001c0017t0018g0052a0007c0018t0018g0053 | 2 | NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-56-13758C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842489 | ||||||
| chr6:39842491
|
G | T | 10 | a0001c0001t0001g0118a0001c0002t0002g0278a0001c0004t0026g0027others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-13756G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842491 | ||||||
| chr6:39842544
|
A | G | 2 | a0001c0004t0035g0126a0001c0008t0005g0101 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-13703A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842544 | ||||||
| chr6:39842549
|
C | G | 2 | a0001c0004t0035g0126a0001c0008t0005g0101 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-13698C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842549 | ||||||
| chr6:39842581
|
C | T | 3 | a0001c0001t0036g0225a0001c0002t0002g0132a0005c0023t0007g0233 | 3 | HG01934.hp2 HG02004.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-56-13666C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842581 | ||||||
| chr6:39842607
|
G | A | 1 | a0004c0030t0001g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-56-13640G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842607 | ||||||
| chr6:39842690
|
G | A | 135 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(132): Show | 135 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.-56-13557G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842690 | ||||||
| chr6:39842844
|
C | A | 1 | a0001c0006t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-13403C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842844 | ||||||
| chr6:39842882
|
T | C | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-56-13365T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842882 | ||||||
| chr6:39842891
|
C | T | 11 | a0001c0001t0001g0106a0001c0001t0001g0203a0001c0001t0001g0223others(8): Show | 11 | HG00621.hp2 NA18747.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-13356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842891 | ||||||
| chr6:39843251
|
T | C | 1 | a0001c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-56-12996T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843251 | ||||||
| chr6:39843280
|
A | G | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-56-12967A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843280 | ||||||
| chr6:39843300
|
G | A | 1 | a0006c0021t0001g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-56-12947G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843300 | ||||||
| chr6:39843381
|
G | A | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-56-12866G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843381 | ||||||
| chr6:39843384
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0112a0001c0001t0001g0118others(42): Show | 45 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-56-12863G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843384 | ||||||
| chr6:39843384
|
G | T | 1 | a0001c0045t0002g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-56-12863G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843384 | ||||||
| chr6:39843521
|
G | T | 1 | a0001c0004t0026g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-56-12726G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843521 | ||||||
| chr6:39843525
|
G | A | 20 | a0001c0001t0001g0112a0001c0001t0001g0118a0001c0001t0001g0208others(17): Show | 20 | HG01255.hp2 HG01361.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-56-12722G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843525 | ||||||
| chr6:39843564
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-56-12683C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843564 | ||||||
| chr6:39843569
|
C | G | 29 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0251others(26): Show | 29 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.-56-12678C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843569 | ||||||
| chr6:39843626
|
T | C | 113 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0075others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-56-12621T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843626 | ||||||
| chr6:39843769
|
C | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0251others(26): Show | 29 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.-56-12478C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843769 | ||||||
| chr6:39843776
|
G | C | 175 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0065others(172): Show | 175 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.-56-12471G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843776 | ||||||
| chr6:39843791
|
G | C | 208 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0034others(205): Show | 208 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.-56-12456G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843791 | ||||||
| chr6:39843836
|
A | T | 1 | a0001c0032t0009g0168 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-12411A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843836 | ||||||
| chr6:39844037
|
A | C | 12 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(9): Show | 12 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-12210A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844037 | ||||||
| chr6:39844107
|
T | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0065others(156): Show | 159 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.-56-12140T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844107 | ||||||
| chr6:39844329
|
C | T | 12 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(9): Show | 12 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-11918C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844329 | ||||||
| chr6:39844371
|
G | GAC | 15 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(12): Show | 15 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-11855_-56-1185 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39844371 | |||||
| chr6:39844371
|
G | GACAC | 32 | a0001c0001t0001g0131a0001c0001t0001g0151a0001c0001t0001g0183others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-56-11857_-56-1185 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39844371 | |||||
| chr6:39844371
|
GAC | G | 12 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(9): Show | 12 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-11855_-56-1185 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39844371 | |||||
| chr6:39844411
|
C | A | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-56-11836C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844411 | ||||||
| chr6:39844517
|
C | T | 7 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0025g0031others(4): Show | 7 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-11730C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844517 | ||||||
| chr6:39844850
|
T | C | 15 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(12): Show | 15 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-11397T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844850 | ||||||
| chr6:39844905
|
A | G | 156 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0065others(153): Show | 156 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-56-11342A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844905 | ||||||
| chr6:39844921
|
T | C | 2 | a0001c0032t0009g0168a0001c0044t0022g0114 | 2 | HG01361.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-56-11326T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844921 | ||||||
| chr6:39844983
|
CACACACA others(2): Show |
C | 12 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(9): Show | 12 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-11255_-56-1124 others(13): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39844983 | |||||
| chr6:39845232
|
G | A | 7 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(4): Show | 7 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-11015G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845232 | ||||||
| chr6:39845253
|
C | T | 1 | a0001c0003t0003g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-10994C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845253 | ||||||
| chr6:39845254
|
G | A | 1 | a0001c0009t0029g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-56-10993G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845254 | ||||||
| chr6:39845256
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-56-10991A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845256 | ||||||
| chr6:39845275
|
A | G | 5 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0136others(2): Show | 5 | HG01943.hp2 HG01952.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-10972A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845275 | ||||||
| chr6:39845284
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-56-10963A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845284 | ||||||
| chr6:39845326
|
CAT | C | 5 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-10919_-56-1091 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845326 | |||||
| chr6:39845345
|
T | TCACACAT others(1517): Show |
3 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051 | 3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10901_-56-1090 others(1528): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845345 | |||||
| chr6:39845350
|
T | C | 3 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051 | 3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10897T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845350 | ||||||
| chr6:39845364
|
G | A | 3 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051 | 3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10883G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845364 | ||||||
| chr6:39845366
|
A | ATACCATA others(356): Show |
3 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051 | 3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10881_-56-1088 others(367): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845366 | ||||||
| chr6:39845369
|
A | AACCCCAT others(1870): Show |
7 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1881): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1881): Show |
11 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1892): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1877): Show |
3 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0026t0001g0280 | 3 | HG01884.hp1 HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1888): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1891): Show |
1 | a0014c0040t0002g0230 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1882): Show |
1 | a0001c0001t0010g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1893): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
1 | a0001c0002t0002g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1893): Show |
1 | a0001c0007t0003g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1904): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1881): Show |
1 | a0001c0003t0003g0290 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1892): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1891): Show |
1 | a0001c0003t0007g0001 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1891): Show |
9 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0002t0002g0107others(6): Show | 9 | NA18944.hp1 NA18949.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1880): Show |
1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1891): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1882): Show |
59 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0039others(56): Show | 59 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1893): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1871): Show |
2 | a0001c0001t0001g0224a0001c0004t0004g0061 | 2 | NA18960.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1882): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1880): Show |
3 | a0001c0001t0001g0164a0001c0001t0001g0231a0001c0001t0001g0240 | 3 | HG03017.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1891): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1877): Show |
1 | a0001c0001t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1888): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
1 | a0001c0003t0003g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
45 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1898): Show |
1 | a0001c0007t0013g0082 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1909): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1887): Show |
1 | a0001c0009t0009g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1898): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
16 | a0001c0001t0001g0072a0001c0001t0001g0105a0001c0001t0001g0127others(13): Show | 16 | HG01106.hp1 HG01261.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1878): Show |
1 | a0009c0041t0014g0147 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1889): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1885): Show |
1 | a0001c0004t0035g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1896): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
2 | a0001c0004t0003g0115a0017c0019t0003g0036 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1891): Show |
72 | a0001c0001t0001g0022a0001c0001t0001g0075a0001c0001t0001g0155others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1880): Show |
1 | a0001c0002t0038g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1891): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1887): Show |
1 | a0001c0002t0002g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1898): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1896): Show |
8 | a0001c0007t0013g0064a0001c0007t0013g0207a0001c0007t0013g0246others(5): Show | 8 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1907): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1891): Show |
1 | a0001c0002t0002g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1887): Show |
3 | a0001c0002t0002g0038a0001c0003t0003g0116a0013c0038t0009g0041 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1898): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0227 | 2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1894): Show |
3 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080 | 3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1905): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1887): Show |
1 | a0001c0033t0001g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1898): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
2 | a0004c0020t0001g0277a0006c0021t0001g0297 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
6 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0251others(3): Show | 6 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
12 | a0001c0001t0019g0050a0001c0001t0019g0121a0001c0005t0011g0030others(9): Show | 12 | HG01081.hp1 HG01361.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1885): Show |
1 | a0001c0001t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1896): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1885): Show |
6 | a0001c0001t0001g0123a0001c0001t0025g0031a0001c0002t0002g0026others(3): Show | 6 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1896): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1883): Show |
1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1894): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1872): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0208 | 2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1883): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
1 | a0018c0047t0001g0066 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
1 | a0001c0003t0003g0216 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
1 | a0001c0032t0009g0168 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | AACCCCAT others(1889): Show |
1 | a0001c0004t0007g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | |||||
| chr6:39845369
|
A | C | 3 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051 | 3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10878A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845369 | ||||||
| chr6:39845440
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-56-10807C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845440 | ||||||
| chr6:39845441
|
G | A | 3 | a0001c0009t0009g0111a0001c0009t0009g0128a0001c0009t0029g0173 | 3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-56-10806G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845441 | ||||||
| chr6:39845495
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0112others(42): Show | 45 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.-56-10752G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845495 | ||||||
| chr6:39845514
|
A | AC | 6 | a0001c0003t0007g0016a0001c0004t0021g0060a0001c0004t0021g0100others(3): Show | 6 | HG01175.hp1 HG01243.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-10731dupC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845514 | |||||
| chr6:39845519
|
A | G | 7 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10728A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845519 | ||||||
| chr6:39845592
|
C | G | 2 | a0001c0003t0007g0001a0014c0040t0002g0230 | 2 | HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-56-10655C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845592 | ||||||
| chr6:39845626
|
T | C | 45 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0112others(42): Show | 45 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.-56-10621T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845626 | ||||||
| chr6:39845729
|
G | T | 1 | a0001c0007t0013g0082 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-56-10518G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845729 | ||||||
| chr6:39845755
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-56-10492G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845755 | ||||||
| chr6:39845757
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-56-10490T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845757 | ||||||
| chr6:39845777
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0112others(42): Show | 45 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.-56-10470G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845777 | ||||||
| chr6:39845784
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-56-10463A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845784 | ||||||
| chr6:39845875
|
C | T | 1 | a0001c0006t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-56-10372C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845875 | ||||||
| chr6:39845920
|
A | G | 7 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0025g0031others(4): Show | 7 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10327A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845920 | ||||||
| chr6:39846018
|
C | T | 92 | a0001c0001t0001g0022a0001c0001t0001g0065a0001c0001t0001g0075others(89): Show | 92 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-56-10229C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846018 | ||||||
| chr6:39846059
|
A | G | 3 | a0001c0004t0003g0115a0001c0033t0001g0044a0017c0019t0003g0036 | 3 | HG02615.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-56-10188A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846059 | ||||||
| chr6:39846207
|
C | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0065others(104): Show | 107 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-56-10040C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846207 | ||||||
| chr6:39846216
|
C | T | 1 | a0001c0003t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-10031C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846216 | ||||||
| chr6:39846339
|
C | A | 2 | a0004c0020t0001g0277a0006c0021t0001g0297 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-9908C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846339 | ||||||
| chr6:39846344
|
T | C | 1 | a0001c0003t0003g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-9903T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846344 | ||||||
| chr6:39846350
|
G | A | 5 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0136others(2): Show | 5 | HG01943.hp2 HG01952.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-9897G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846350 | ||||||
| chr6:39846504
|
T | C | 156 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0065others(153): Show | 156 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-56-9743T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846504 | ||||||
| chr6:39846572
|
C | T | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-56-9675C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846572 | ||||||
| chr6:39846633
|
C | A | 156 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0065others(153): Show | 156 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-56-9614C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846633 | ||||||
| chr6:39846699
|
C | CT | 6 | a0001c0001t0001g0211a0001c0008t0005g0286a0001c0013t0023g0169others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-9533dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39846699 | |||||
| chr6:39846699
|
CT | C | 106 | a0001c0001t0001g0022a0001c0001t0001g0065a0001c0001t0001g0075others(103): Show | 106 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-56-9533delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39846699 | |||||
| chr6:39846699
|
CTT | C | 11 | a0001c0001t0001g0181a0001c0003t0003g0196a0001c0004t0006g0074others(8): Show | 11 | NA18747.hp1 NA18939.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-9534_-56-9533d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39846699 | |||||
| chr6:39846727
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0112a0001c0001t0001g0118others(13): Show | 16 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-9520C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846727 | ||||||
| chr6:39846728
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-56-9519G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846728 | ||||||
| chr6:39846733
|
G | T | 1 | a0001c0002t0002g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-56-9514G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846733 | ||||||
| chr6:39846947
|
C | T | 1 | a0001c0006t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-9300C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846947 | ||||||
| chr6:39847157
|
G | A | 3 | a0001c0001t0001g0178a0001c0002t0002g0019a0001c0002t0002g0020 | 3 | NA18963.hp1 NA18972.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-56-9090G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847157 | ||||||
| chr6:39847290
|
G | A | 1 | a0001c0004t0004g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-56-8957G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847290 | ||||||
| chr6:39847306
|
C | T | 6 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-8941C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847306 | ||||||
| chr6:39847333
|
G | C | 1 | a0001c0001t0010g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56-8914G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847333 | ||||||
| chr6:39847396
|
G | C | 14 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-8851G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847396 | ||||||
| chr6:39847409
|
G | A | 14 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(11): Show | 14 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-8838G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847409 | ||||||
| chr6:39847454
|
G | C | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-56-8793G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847454 | ||||||
| chr6:39847654
|
C | T | 2 | a0001c0001t0019g0050a0001c0001t0019g0121 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-56-8593C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847654 | ||||||
| chr6:39847655
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-56-8592G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847655 | ||||||
| chr6:39847797
|
C | A | 14 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(11): Show | 14 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-8450C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847797 | ||||||
| chr6:39847819
|
C | T | 88 | a0001c0001t0001g0022a0001c0001t0001g0065a0001c0001t0001g0075others(85): Show | 88 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-56-8428C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847819 | ||||||
| chr6:39847836
|
C | G | 14 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(11): Show | 14 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-8411C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847836 | ||||||
| chr6:39847987
|
G | A | 4 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-8260G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847987 | ||||||
| chr6:39848013
|
A | G | 6 | a0001c0002t0002g0045a0001c0002t0002g0097a0001c0002t0002g0238others(3): Show | 6 | HG00423.hp2 NA18971.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-8234A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848013 | ||||||
| chr6:39848137
|
C | T | 2 | a0001c0032t0009g0168a0001c0044t0022g0114 | 2 | HG01361.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-56-8110C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848137 | ||||||
| chr6:39848142
|
CTTCA | C | 7 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(4): Show | 7 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-8102_-56-8099d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39848142 | |||||
| chr6:39848157
|
T | C | 32 | a0001c0001t0001g0009a0001c0001t0001g0112a0001c0001t0001g0118others(29): Show | 32 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-56-8090T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848157 | ||||||
| chr6:39848240
|
C | T | 1 | a0001c0022t0020g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-56-8007C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848240 | ||||||
| chr6:39848357
|
T | C | 59 | a0001c0001t0001g0022a0001c0001t0001g0075a0001c0001t0001g0155others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.-56-7890T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848357 | ||||||
| chr6:39848428
|
CTT | C | 3 | a0001c0016t0004g0054a0001c0017t0018g0052a0007c0018t0018g0053 | 3 | NA18994.hp2 NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-56-7817_-56-7816d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39848428 | |||||
| chr6:39848531
|
T | C | 1 | a0001c0033t0001g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-7716T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848531 | ||||||
| chr6:39848537
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-56-7710G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848537 | ||||||
| chr6:39848543
|
C | T | 1 | a0001c0008t0005g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-56-7704C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848543 | ||||||
| chr6:39848545
|
T | C | 14 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(11): Show | 14 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-7702T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848545 | ||||||
| chr6:39848617
|
G | A | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-7630G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848617 | ||||||
| chr6:39848858
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0275 | 2 | NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-56-7389T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848858 | ||||||
| chr6:39848865
|
C | A | 1 | a0001c0004t0031g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-56-7382C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848865 | ||||||
| chr6:39848891
|
G | A | 88 | a0001c0001t0001g0022a0001c0001t0001g0065a0001c0001t0001g0093others(85): Show | 88 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-56-7356G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848891 | ||||||
| chr6:39848929
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0112a0001c0001t0001g0118others(15): Show | 18 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-56-7318C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848929 | ||||||
| chr6:39848959
|
C | T | 1 | a0001c0007t0015g0057 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-56-7288C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848959 | ||||||
| chr6:39849008
|
T | TG | 4 | a0003c0011t0001g0003a0003c0011t0001g0005a0003c0011t0001g0006others(1): Show | 4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-7236dupG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39849008 | |||||
| chr6:39849122
|
C | G | 1 | a0001c0002t0002g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-56-7125C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849122 | ||||||
| chr6:39849395
|
G | A | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56-6852G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849395 | ||||||
| chr6:39849407
|
G | T | 1 | a0014c0040t0002g0230 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-56-6840G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849407 | ||||||
| chr6:39849536
|
T | C | 106 | a0001c0001t0001g0022a0001c0001t0001g0065a0001c0001t0001g0093others(103): Show | 106 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-56-6711T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849536 | ||||||
| chr6:39849777
|
G | T | 2 | a0001c0003t0003g0287a0001c0003t0003g0289 | 2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-56-6470G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849777 | ||||||
| chr6:39849982
|
C | T | 1 | a0001c0003t0003g0129 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-56-6265C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849982 | ||||||
| chr6:39850029
|
T | TCCCAGC | 56 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0118others(53): Show | 56 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.-56-6206_-56-6201d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39850029 | |||||
| chr6:39850029
|
T | TCCCAGCC others(5): Show |
13 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(10): Show | 13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-6212_-56-6201d others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39850029 | |||||
| chr6:39850124
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0251others(10): Show | 13 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-56-6123C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850124 | ||||||
| chr6:39850239
|
C | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0118others(19): Show | 22 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-56-6008C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850239 | ||||||
| chr6:39850399
|
C | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0164a0001c0001t0001g0231others(1): Show | 4 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-5848C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850399 | ||||||
| chr6:39850439
|
T | G | 2 | a0001c0003t0007g0016a0001c0031t0040g0143 | 2 | HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-56-5808T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850439 | ||||||
| chr6:39850509
|
G | A | 7 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-5738G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850509 | ||||||
| chr6:39850598
|
T | C | 161 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0065others(158): Show | 161 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-5649T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850598 | ||||||
| chr6:39850665
|
C | A | 1 | a0001c0001t0001g0096 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-56-5582C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850665 | ||||||
| chr6:39850889
|
G | A | 2 | a0001c0001t0001g0189a0001c0005t0037g0062 | 2 | NA19007.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-56-5358G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850889 | ||||||
| chr6:39851088
|
T | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0118others(21): Show | 24 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.-56-5159T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851088 | ||||||
| chr6:39851231
|
G | A | 3 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080 | 3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-56-5016G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851231 | ||||||
| chr6:39851368
|
T | A | 10 | a0001c0007t0003g0058a0001c0007t0013g0064a0001c0007t0013g0082others(7): Show | 10 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-4879T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851368 | ||||||
| chr6:39851388
|
G | T | 1 | a0001c0004t0006g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-56-4859G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851388 | ||||||
| chr6:39851430
|
A | C | 4 | a0003c0011t0001g0003a0003c0011t0001g0005a0003c0011t0001g0006others(1): Show | 4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-4817A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851430 | ||||||
| chr6:39851758
|
C | A | 2 | a0004c0020t0001g0277a0006c0021t0001g0297 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-4489C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851758 | ||||||
| chr6:39851760
|
C | T | 3 | a0001c0002t0002g0019a0001c0002t0002g0020a0001c0002t0002g0023 | 3 | HG04228.hp2 NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-56-4487C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851760 | ||||||
| chr6:39851761
|
G | A | 2 | a0001c0003t0003g0176a0001c0004t0003g0102 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-56-4486G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851761 | ||||||
| chr6:39851777
|
G | A | 1 | a0001c0032t0009g0168 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-4470G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851777 | ||||||
| chr6:39851811
|
C | G | 3 | a0001c0009t0009g0111a0001c0009t0009g0128a0001c0009t0029g0173 | 3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-56-4436C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851811 | ||||||
| chr6:39852125
|
C | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0118others(19): Show | 22 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-56-4122C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852125 | ||||||
| chr6:39852187
|
G | A | 3 | a0001c0009t0009g0111a0001c0009t0009g0128a0001c0009t0029g0173 | 3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-56-4060G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852187 | ||||||
| chr6:39852587
|
G | A | 10 | a0001c0007t0003g0058a0001c0007t0013g0064a0001c0007t0013g0082others(7): Show | 10 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-3660G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852587 | ||||||
| chr6:39852644
|
A | G | 1 | a0001c0032t0009g0168 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-3603A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852644 | ||||||
| chr6:39852703
|
C | T | 5 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3544C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852703 | ||||||
| chr6:39852774
|
A | G | 1 | a0001c0002t0002g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-3473A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852774 | ||||||
| chr6:39853039
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0208a0001c0001t0019g0050others(1): Show | 4 | HG01255.hp2 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-3208T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853039 | ||||||
| chr6:39853142
|
G | A | 2 | a0001c0014t0001g0029a0001c0014t0017g0266 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-56-3105G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853142 | ||||||
| chr6:39853224
|
T | A | 9 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-3023T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853224 | ||||||
| chr6:39853579
|
C | T | 161 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0065others(158): Show | 161 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-2668C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853579 | ||||||
| chr6:39853752
|
T | A | 18 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(15): Show | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-56-2495T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853752 | ||||||
| chr6:39853764
|
C | G | 1 | a0001c0032t0009g0168 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-2483C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853764 | ||||||
| chr6:39853895
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0208a0001c0001t0019g0050others(1): Show | 4 | HG01255.hp2 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-2352A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853895 | ||||||
| chr6:39853965
|
C | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0251others(10): Show | 13 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-56-2282C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853965 | ||||||
| chr6:39854268
|
G | A | 2 | a0001c0014t0001g0029a0001c0014t0017g0266 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-56-1979G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854268 | ||||||
| chr6:39854317
|
T | G | 13 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(10): Show | 13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-1930T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854317 | ||||||
| chr6:39854343
|
A | G | 174 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(171): Show | 174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-56-1904A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854343 | ||||||
| chr6:39854395
|
G | A | 5 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-1852G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854395 | ||||||
| chr6:39854407
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0072a0001c0001t0001g0105others(19): Show | 22 | HG00735.hp1 HG01106.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-56-1840T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854407 | ||||||
| chr6:39854413
|
T | C | 4 | a0001c0004t0021g0060a0001c0004t0021g0100a0001c0004t0031g0294others(1): Show | 4 | HG02451.hp1 HG03516.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1834T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854413 | ||||||
| chr6:39854443
|
G | A | 187 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(184): Show | 187 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.-56-1804G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854443 | ||||||
| chr6:39854648
|
G | T | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1599G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854648 | ||||||
| chr6:39854958
|
A | G | 1 | a0001c0004t0035g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-56-1289A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854958 | ||||||
| chr6:39854966
|
G | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0118others(27): Show | 30 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-56-1281G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854966 | ||||||
| chr6:39855422
|
A | G | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 186 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.-56-825A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855422 | ||||||
| chr6:39855425
|
C | T | 9 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-822C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855425 | ||||||
| chr6:39855443
|
A | G | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 186 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.-56-804A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855443 | ||||||
| chr6:39855448
|
C | G | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 186 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.-56-799C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855448 | ||||||
| chr6:39855525
|
C | G | 4 | a0001c0004t0004g0070a0002c0010t0002g0095a0002c0010t0002g0236others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-722C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855525 | ||||||
| chr6:39855768
|
C | T | 13 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(10): Show | 13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-479C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855768 | ||||||
| chr6:39855831
|
G | C | 1 | a0001c0003t0039g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-56-416G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855831 | ||||||
| chr6:39855863
|
T | C | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-384T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855863 | ||||||
| chr6:39855892
|
T | G | 45 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-56-355T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855892 | ||||||
| chr6:39855895
|
G | A | 1 | a0001c0012t0002g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-56-352G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855895 | ||||||
| chr6:39855962
|
C | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0118others(19): Show | 22 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-56-285C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855962 | ||||||
| chr6:39856649
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.168+179T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856649 | ||||||
| chr6:39856765
|
A | C | 13 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(10): Show | 13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+295A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856765 | ||||||
| chr6:39856791
|
G | T | 168 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(165): Show | 168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.168+321G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856791 | ||||||
| chr6:39856872
|
A | G | 9 | a0001c0001t0001g0181a0001c0003t0003g0196a0001c0004t0004g0205others(6): Show | 9 | NA18939.hp1 NA18939.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+402A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856872 | ||||||
| chr6:39856905
|
G | T | 13 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(10): Show | 13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+435G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856905 | ||||||
| chr6:39857029
|
T | C | 9 | a0001c0001t0019g0050a0001c0001t0019g0121a0001c0005t0011g0030others(6): Show | 9 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+559T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857029 | ||||||
| chr6:39857066
|
G | A | 21 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0118others(18): Show | 21 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.168+596G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857066 | ||||||
| chr6:39857102
|
G | A | 3 | a0001c0009t0009g0111a0001c0009t0009g0128a0001c0009t0029g0173 | 3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.168+632G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857102 | ||||||
| chr6:39857132
|
C | T | 1 | a0001c0005t0004g0081 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.168+662C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857132 | ||||||
| chr6:39857303
|
A | G | 7 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+833A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857303 | ||||||
| chr6:39857584
|
A | G | 1 | a0010c0028t0004g0291 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.168+1114A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857584 | ||||||
| chr6:39857744
|
G | C | 7 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+1274G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857744 | ||||||
| chr6:39857771
|
C | T | 4 | a0001c0007t0003g0058a0001c0007t0013g0064a0001c0007t0013g0207others(1): Show | 4 | NA18945.hp1 NA18956.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+1301C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857771 | ||||||
| chr6:39857799
|
G | C | 9 | a0001c0007t0003g0058a0001c0007t0013g0064a0001c0007t0013g0207others(6): Show | 9 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+1329G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857799 | ||||||
| chr6:39857868
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.168+1398C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857868 | ||||||
| chr6:39857869
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.168+1399T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857869 | ||||||
| chr6:39858090
|
G | T | 13 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0001t0001g0178others(10): Show | 13 | HG02083.hp2 NA18944.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+1620G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858090 | ||||||
| chr6:39858108
|
C | T | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.168+1638C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858108 | ||||||
| chr6:39858154
|
G | T | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.168+1684G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858154 | ||||||
| chr6:39858460
|
A | G | 173 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(170): Show | 173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.168+1990A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858460 | ||||||
| chr6:39858491
|
G | T | 1 | a0001c0008t0005g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168+2021G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858491 | ||||||
| chr6:39858684
|
C | T | 6 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0136others(3): Show | 6 | HG01943.hp2 HG01952.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2214C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858684 | ||||||
| chr6:39858767
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.169-2161G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858767 | ||||||
| chr6:39859047
|
A | T | 9 | a0001c0007t0003g0058a0001c0007t0013g0064a0001c0007t0013g0207others(6): Show | 9 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-1881A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39859047 | ||||||
| chr6:39859714
|
A | G | 224 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(221): Show | 224 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.169-1214A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39859714 | ||||||
| chr6:39859951
|
TAA | T | 8 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-975_169-974del others(2): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr6 | 39859951 | |||||
| chr6:39859958
|
T | G | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169-970T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39859958 | ||||||
| chr6:39859966
|
T | G | 7 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0025g0031others(4): Show | 7 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-962T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39859966 | ||||||
| chr6:39860028
|
A | G | 173 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(170): Show | 173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.169-900A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860028 | ||||||
| chr6:39860031
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.169-897C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860031 | ||||||
| chr6:39860263
|
T | C | 1 | a0001c0002t0002g0144 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.169-665T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860263 | ||||||
| chr6:39860301
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.169-627A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860301 | ||||||
| chr6:39860342
|
C | T | 1 | a0001c0002t0002g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.169-586C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860342 | ||||||
| chr6:39860405
|
A | G | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.169-523A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860405 | ||||||
| chr6:39860432
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0234others(11): Show | 14 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-496G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860432 | ||||||
| chr6:39860503
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.169-425A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860503 | ||||||
| chr6:39860817
|
A | T | 140 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(137): Show | 140 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.169-111A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860817 | ||||||
| chr6:39860853
|
A | G | 1 | a0001c0004t0006g0074 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.169-75A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860853 | ||||||
| chr6:39861039
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0234others(11): Show | 14 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+22G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861039 | ||||||
| chr6:39861048
|
C | T | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.258+31C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861048 | ||||||
| chr6:39861086
|
A | C | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 186 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.258+69A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861086 | ||||||
| chr6:39861094
|
G | A | 3 | a0001c0009t0009g0111a0001c0009t0009g0128a0001c0009t0029g0173 | 3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.258+77G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861094 | ||||||
| chr6:39861101
|
C | A | 1 | a0001c0026t0001g0280 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.258+84C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861101 | ||||||
| chr6:39861339
|
T | C | 4 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+322T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861339 | ||||||
| chr6:39861340
|
G | A | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.258+323G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861340 | ||||||
| chr6:39861362
|
G | T | 4 | a0003c0011t0001g0003a0003c0011t0001g0005a0003c0011t0001g0006others(1): Show | 4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+345G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861362 | ||||||
| chr6:39861447
|
T | C | 184 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(181): Show | 184 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.258+430T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861447 | ||||||
| chr6:39861499
|
G | A | 7 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+482G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861499 | ||||||
| chr6:39861692
|
G | T | 7 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+675G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861692 | ||||||
| chr6:39861772
|
C | A | 1 | a0001c0003t0003g0290 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.258+755C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861772 | ||||||
| chr6:39861897
|
C | G | 1 | a0001c0007t0013g0082 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.258+880C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861897 | ||||||
| chr6:39862040
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0193others(3): Show | 6 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+1023C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862040 | ||||||
| chr6:39862042
|
A | G | 7 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+1025A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862042 | ||||||
| chr6:39862148
|
G | A | 1 | a0001c0005t0006g0197 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.258+1131G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862148 | ||||||
| chr6:39862160
|
C | T | 1 | a0001c0002t0002g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.258+1143C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862160 | ||||||
| chr6:39862486
|
A | C | 1 | a0001c0004t0007g0237 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.258+1469A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862486 | ||||||
| chr6:39862493
|
AAAAC | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0193a0001c0001t0001g0281others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1496_258+1499d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862493 | |||||
| chr6:39862513
|
C | A | 1 | a0001c0001t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.258+1496C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862513 | ||||||
| chr6:39862541
|
T | C | 183 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(180): Show | 183 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.258+1524T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862541 | ||||||
| chr6:39862753
|
C | T | 3 | a0001c0009t0009g0111a0001c0009t0009g0128a0001c0009t0029g0173 | 3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.259-1680C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862753 | ||||||
| chr6:39862791
|
G | A | 2 | a0001c0001t0001g0220a0012c0034t0001g0232 | 2 | HG01515.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.259-1642G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862791 | ||||||
| chr6:39862792
|
C | T | 1 | a0001c0002t0002g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.259-1641C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862792 | ||||||
| chr6:39862805
|
C | CA | 34 | a0001c0001t0001g0155a0001c0001t0001g0181a0001c0002t0002g0045others(31): Show | 34 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.259-1597dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
C | CAA | 15 | a0001c0001t0001g0213a0001c0002t0002g0007a0001c0002t0002g0018others(12): Show | 15 | HG00438.hp2 HG01123.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-1598_259-1597d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
CA | C | 19 | a0001c0001t0001g0093a0001c0002t0002g0020a0001c0002t0002g0107others(16): Show | 19 | HG01361.hp2 HG02818.hp1 HG02922.hp1 others(16): Show |
intron_variant | MODIFIER | c.259-1597delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
CAA | C | 16 | a0001c0001t0001g0065a0001c0004t0004g0037a0001c0004t0004g0046others(13): Show | 16 | HG01884.hp1 HG02083.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-1598_259-1597d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
CAAA | C | 17 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0001g0087others(14): Show | 17 | HG00423.hp1 HG01123.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.259-1599_259-1597d others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
CAAAA | C | 126 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0022others(123): Show | 126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.259-1600_259-1597d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
CAAAAA | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0072others(32): Show | 35 | HG00741.hp2 HG01081.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.259-1601_259-1597d others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
CAAAAAA | C | 6 | a0001c0008t0005g0293a0001c0009t0009g0111a0001c0009t0009g0128others(3): Show | 6 | HG02630.hp1 HG02895.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1602_259-1597d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
CAAAAAAA others(6): Show |
C | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1609_259-1597d others(15): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862805
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-1612_259-1597d others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | |||||
| chr6:39862811
|
A | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0208 | 2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.259-1622A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862811 | ||||||
| chr6:39863112
|
C | T | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-1321C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863112 | ||||||
| chr6:39863224
|
G | A | 1 | a0014c0040t0002g0230 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.259-1209G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863224 | ||||||
| chr6:39863260
|
A | G | 15 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0002t0002g0107others(12): Show | 15 | HG02083.hp2 HG02129.hp1 HG04184.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-1173A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863260 | ||||||
| chr6:39863363
|
T | A | 1 | a0001c0004t0031g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.259-1070T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863363 | ||||||
| chr6:39863691
|
A | G | 172 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(169): Show | 172 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.259-742A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863691 | ||||||
| chr6:39863902
|
A | C | 10 | a0001c0002t0002g0038a0001c0003t0003g0116a0001c0004t0003g0115others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-531A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863902 | ||||||
| chr6:39864094
|
G | T | 1 | a0001c0002t0002g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.259-339G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39864094 | ||||||
| chr6:39864164
|
TA | T | 7 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(4): Show | 7 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-263delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39864164 | |||||
| chr6:39864221
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.259-212C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39864221 | ||||||
| chr6:39864335
|
A | G | 177 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.259-98A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39864335 | ||||||
| chr6:39864587
|
C | A | 7 | a0001c0004t0004g0205a0001c0004t0006g0074a0001c0004t0006g0089others(4): Show | 7 | NA18939.hp2 NA18945.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+80C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 4/24 | chr6 | 39864587 | ||||||
| chr6:39864587
|
C | G | 228 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(225): Show | 228 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.333+80C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 4/24 | chr6 | 39864587 | ||||||
| chr6:39864774
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.334-206G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 4/24 | chr6 | 39864774 | ||||||
| chr6:39865116
|
A | G | 3 | a0001c0002t0002g0038a0001c0003t0003g0116a0013c0038t0009g0041 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.428+42A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865116 | ||||||
| chr6:39865188
|
T | C | 213 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 213 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.428+114T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865188 | ||||||
| chr6:39865227
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.428+153C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865227 | ||||||
| chr6:39865430
|
C | T | 5 | a0001c0008t0005g0101a0001c0008t0005g0165a0001c0008t0005g0286others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865430 | ||||||
| chr6:39865462
|
C | G | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.428+388C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865462 | ||||||
| chr6:39865486
|
C | T | 11 | a0001c0006t0001g0040a0001c0006t0001g0152a0001c0006t0001g0158others(8): Show | 11 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.428+412C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865486 | ||||||
| chr6:39865547
|
G | A | 1 | a0001c0009t0009g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.428+473G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865547 | ||||||
| chr6:39865551
|
T | C | 1 | a0001c0004t0004g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.428+477T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865551 | ||||||
| chr6:39865631
|
G | A | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+557G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865631 | ||||||
| chr6:39865695
|
T | C | 181 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(178): Show | 181 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.428+621T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865695 | ||||||
| chr6:39865898
|
C | T | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+824C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865898 | ||||||
| chr6:39865911
|
T | C | 2 | a0001c0002t0002g0145a0001c0002t0002g0263 | 2 | HG01943.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.428+837T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865911 | ||||||
| chr6:39866142
|
C | T | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+1068C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866142 | ||||||
| chr6:39866235
|
A | G | 227 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(224): Show | 227 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.428+1161A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866235 | ||||||
| chr6:39866313
|
T | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-1197T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866313 | ||||||
| chr6:39866365
|
TA | T | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-1138delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr6 | 39866365 | |||||
| chr6:39866366
|
A | G | 1 | a0001c0003t0003g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.429-1144A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866366 | ||||||
| chr6:39866373
|
T | C | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-1137T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866373 | ||||||
| chr6:39866393
|
G | C | 53 | a0001c0001t0001g0155a0001c0001t0001g0213a0001c0001t0001g0274others(50): Show | 53 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.429-1117G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866393 | ||||||
| chr6:39866430
|
G | A | 1 | a0001c0012t0002g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.429-1080G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866430 | ||||||
| chr6:39866461
|
A | G | 4 | a0003c0011t0001g0003a0003c0011t0001g0005a0003c0011t0001g0006others(1): Show | 4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-1049A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866461 | ||||||
| chr6:39866538
|
A | G | 180 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(177): Show | 180 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.429-972A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866538 | ||||||
| chr6:39866559
|
T | C | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-951T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866559 | ||||||
| chr6:39866610
|
A | G | 57 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(54): Show | 57 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.429-900A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866610 | ||||||
| chr6:39866615
|
G | T | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.429-895G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866615 | ||||||
| chr6:39866621
|
C | A | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 226 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.429-889C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866621 | ||||||
| chr6:39866809
|
G | A | 1 | a0001c0004t0006g0089 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.429-701G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866809 | ||||||
| chr6:39866936
|
T | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0109a0001c0001t0010g0084 | 3 | HG02015.hp1 HG02523.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.429-574T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866936 | ||||||
| chr6:39867456
|
AGT | A | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-51_429-50delGT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr6 | 39867456 | |||||
| chr6:39867500
|
T | C | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-10T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39867500 | ||||||
| chr6:39867936
|
T | G | 1 | a0018c0047t0001g0066 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.762+93T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39867936 | ||||||
| chr6:39867978
|
G | C | 1 | a0001c0001t0008g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.762+135G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39867978 | ||||||
| chr6:39868020
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.762+177T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868020 | ||||||
| chr6:39868072
|
T | C | 146 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(143): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.762+229T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868072 | ||||||
| chr6:39868076
|
T | C | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.762+233T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868076 | ||||||
| chr6:39868331
|
G | A | 224 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(221): Show | 224 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.762+488G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868331 | ||||||
| chr6:39868495
|
T | G | 224 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(221): Show | 224 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.763-328T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868495 | ||||||
| chr6:39868605
|
G | A | 1 | a0001c0032t0009g0168 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.763-218G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868605 | ||||||
| chr6:39868681
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.763-142G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868681 | ||||||
| chr6:39868799
|
G | A | 11 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(8): Show | 11 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.763-24G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868799 | ||||||
| chr6:39868997
|
A | T | 3 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0026t0001g0280 | 3 | HG01884.hp1 HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.873+64A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39868997 | ||||||
| chr6:39869014
|
A | G | 8 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0025g0031others(5): Show | 8 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+81A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869014 | ||||||
| chr6:39869060
|
C | A | 1 | a0001c0002t0002g0254 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.873+127C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869060 | ||||||
| chr6:39869063
|
C | T | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.873+130C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869063 | ||||||
| chr6:39869200
|
C | T | 17 | a0001c0001t0001g0048a0001c0001t0001g0065a0001c0001t0001g0073others(14): Show | 17 | HG01433.hp1 HG01496.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.873+267C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869200 | ||||||
| chr6:39869307
|
G | A | 1 | a0001c0003t0003g0014 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.873+374G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869307 | ||||||
| chr6:39869310
|
C | T | 1 | a0001c0003t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.873+377C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869310 | ||||||
| chr6:39869325
|
C | T | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.873+392C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869325 | ||||||
| chr6:39869421
|
C | T | 9 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.873+488C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869421 | ||||||
| chr6:39869443
|
C | T | 33 | a0001c0001t0001g0235a0001c0001t0010g0015a0001c0003t0003g0002others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.873+510C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869443 | ||||||
| chr6:39869519
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.873+586G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869519 | ||||||
| chr6:39869576
|
G | A | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.873+643G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869576 | ||||||
| chr6:39869601
|
C | A | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.873+668C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869601 | ||||||
| chr6:39869666
|
T | C | 1 | a0001c0004t0035g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.874-674T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869666 | ||||||
| chr6:39869753
|
C | CT | 15 | a0001c0001t0001g0065a0001c0001t0001g0274a0001c0002t0002g0018others(12): Show | 15 | HG00642.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.874-560dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | |||||
| chr6:39869753
|
CT | C | 70 | a0001c0001t0001g0131a0001c0001t0001g0151a0001c0001t0001g0183others(67): Show | 70 | HG00423.hp1 HG00621.hp1 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.874-560delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | |||||
| chr6:39869753
|
CTT | C | 82 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0022others(79): Show | 82 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.874-561_874-560del others(2): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | |||||
| chr6:39869753
|
CTTT | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0048a0001c0001t0001g0073others(9): Show | 12 | HG01433.hp1 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.874-562_874-560del others(3): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | |||||
| chr6:39869753
|
CTTTTTT | C | 7 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0025g0031others(4): Show | 7 | HG02922.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.874-565_874-560del others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | |||||
| chr6:39869753
|
CTTTTTTT others(1): Show |
C | 16 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0234others(13): Show | 16 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.874-567_874-560del others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | |||||
| chr6:39869753
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0006t0001g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.874-572_874-560del others(13): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | |||||
| chr6:39869755
|
T | G | 2 | a0001c0001t0019g0050a0001c0001t0019g0121 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.874-585T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869755 | ||||||
| chr6:39869756
|
T | G | 5 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(2): Show | 5 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.874-584T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869756 | ||||||
| chr6:39869780
|
T | A | 3 | a0001c0002t0002g0253a0001c0003t0003g0110a0001c0003t0003g0270 | 3 | HG02040.hp1 NA18952.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.874-560T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869780 | ||||||
| chr6:39869780
|
T | TTA | 8 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(5): Show | 8 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.874-560_874-559ins others(2): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869780 | ||||||
| chr6:39869781
|
A | T | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.874-559A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869781 | ||||||
| chr6:39869804
|
TG | T | 14 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0002t0002g0107others(11): Show | 14 | HG02083.hp2 HG02129.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-533delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869804 | |||||
| chr6:39869905
|
T | G | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-435T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869905 | ||||||
| chr6:39870105
|
G | A | 3 | a0001c0005t0004g0063a0001c0005t0004g0081a0001c0005t0004g0212 | 3 | NA18952.hp2 NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.874-235G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39870105 | ||||||
| chr6:39870127
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.874-213A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39870127 | ||||||
| chr6:39870506
|
T | C | 1 | a0001c0002t0002g0253 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.977+63T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870506 | ||||||
| chr6:39870585
|
G | A | 3 | a0001c0002t0002g0038a0001c0003t0003g0116a0001c0006t0001g0032 | 3 | HG02451.hp2 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.977+142G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870585 | ||||||
| chr6:39870621
|
C | T | 1 | a0001c0002t0002g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.977+178C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870621 | ||||||
| chr6:39870693
|
G | C | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.977+250G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870693 | ||||||
| chr6:39870720
|
C | T | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 226 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.977+277C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870720 | ||||||
| chr6:39870849
|
C | T | 40 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0086others(37): Show | 40 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.977+406C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870849 | ||||||
| chr6:39871230
|
T | C | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.978-276T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871230 | ||||||
| chr6:39871232
|
A | T | 1 | a0001c0033t0001g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.978-274A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871232 | ||||||
| chr6:39871291
|
C | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0123others(22): Show | 25 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.978-215C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871291 | ||||||
| chr6:39871311
|
G | A | 1 | a0001c0036t0022g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.978-195G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871311 | ||||||
| chr6:39871388
|
T | C | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 226 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.978-118T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871388 | ||||||
| chr6:39871596
|
G | A | 3 | a0003c0011t0001g0003a0003c0011t0001g0005a0003c0011t0001g0006 | 3 | HG02970.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1044+24G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39871596 | ||||||
| chr6:39871651
|
C | T | 1 | a0001c0022t0020g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1044+79C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39871651 | ||||||
| chr6:39871675
|
G | A | 1 | a0001c0002t0002g0283 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1044+103G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39871675 | ||||||
| chr6:39871681
|
T | G | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+109T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39871681 | ||||||
| chr6:39872033
|
C | T | 4 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+461C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872033 | ||||||
| chr6:39872228
|
C | A | 10 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(7): Show | 10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+656C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872228 | ||||||
| chr6:39872286
|
A | G | 4 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+714A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872286 | ||||||
| chr6:39872298
|
A | G | 1 | a0011c0029t0001g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1044+726A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872298 | ||||||
| chr6:39872306
|
C | T | 1 | a0001c0007t0013g0082 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1044+734C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872306 | ||||||
| chr6:39872387
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0010g0269 | 2 | HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1044+815G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872387 | ||||||
| chr6:39872747
|
G | A | 1 | a0001c0002t0002g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1045-491G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872747 | ||||||
| chr6:39872816
|
G | T | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1045-422G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872816 | ||||||
| chr6:39872833
|
T | TG | 182 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 182 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1045-405_1045-404i others(3): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872833 | ||||||
| chr6:39872899
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0227 | 2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1045-339A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872899 | ||||||
| chr6:39872922
|
T | C | 3 | a0001c0003t0003g0179a0001c0003t0003g0196a0001c0003t0003g0199 | 3 | HG00621.hp1 HG03017.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1045-316T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872922 | ||||||
| chr6:39873060
|
T | C | 3 | a0001c0003t0016g0122a0001c0003t0016g0206a0001c0003t0016g0284 | 3 | HG02717.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1045-178T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873060 | ||||||
| chr6:39873061
|
A | C | 1 | a0001c0007t0013g0082 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1045-177A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873061 | ||||||
| chr6:39873125
|
G | A | 1 | a0003c0024t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1045-113G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873125 | ||||||
| chr6:39873206
|
C | T | 8 | a0001c0005t0014g0175a0001c0006t0001g0040a0001c0006t0001g0152others(5): Show | 8 | HG00741.hp2 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1045-32C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873206 | ||||||
| chr6:39873214
|
T | A | 4 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-24T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873214 | ||||||
| chr6:39873929
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1162+574A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39873929 | ||||||
| chr6:39874222
|
A | G | 182 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 182 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1162+867A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874222 | ||||||
| chr6:39874607
|
T | C | 15 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(12): Show | 15 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1163-723T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874607 | ||||||
| chr6:39874658
|
C | T | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1163-672C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874658 | ||||||
| chr6:39874685
|
C | A | 2 | a0001c0004t0003g0115a0017c0019t0003g0036 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1163-645C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874685 | ||||||
| chr6:39874686
|
A | G | 3 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080 | 3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1163-644A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874686 | ||||||
| chr6:39874719
|
A | G | 38 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(35): Show | 38 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1163-611A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874719 | ||||||
| chr6:39874907
|
T | G | 1 | a0001c0001t0001g0072 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1163-423T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874907 | ||||||
| chr6:39875004
|
T | C | 1 | a0001c0002t0002g0107 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1163-326T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39875004 | ||||||
| chr6:39875073
|
A | C | 1 | a0001c0008t0005g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1163-257A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39875073 | ||||||
| chr6:39875138
|
C | T | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(166): Show | 169 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1163-192C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39875138 | ||||||
| chr6:39875510
|
C | G | 1 | a0001c0002t0002g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1301+42C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875510 | ||||||
| chr6:39875575
|
C | T | 1 | a0001c0002t0002g0107 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1301+107C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875575 | ||||||
| chr6:39875634
|
A | G | 8 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0025g0031others(5): Show | 8 | HG02895.hp1 HG02922.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301+166A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875634 | ||||||
| chr6:39875739
|
C | A | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 223 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1301+271C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875739 | ||||||
| chr6:39875821
|
G | A | 8 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0025g0031others(5): Show | 8 | HG02895.hp1 HG02922.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301+353G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875821 | ||||||
| chr6:39876446
|
T | C | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 226 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1301+978T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876446 | ||||||
| chr6:39876504
|
C | G | 2 | a0001c0032t0009g0168a0001c0044t0022g0114 | 2 | HG01361.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1301+1036C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876504 | ||||||
| chr6:39876523
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1301+1055C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876523 | ||||||
| chr6:39876557
|
G | A | 1 | a0001c0002t0002g0186 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1301+1089G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876557 | ||||||
| chr6:39876706
|
GGTGTGT | G | 3 | a0003c0011t0001g0003a0003c0011t0001g0005a0003c0011t0001g0006 | 3 | HG02970.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1301+1256_1301+126 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr6 | 39876706 | |||||
| chr6:39876722
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1301+1254T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876722 | ||||||
| chr6:39876724
|
T | TGC | 4 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0025t0034g0300others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+1257_1301+125 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr6 | 39876724 | |||||
| chr6:39876726
|
T | C | 33 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0123others(30): Show | 33 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1301+1258T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876726 | ||||||
| chr6:39876726
|
T | TGC | 188 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(185): Show | 188 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1301+1259_1301+126 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr6 | 39876726 | |||||
| chr6:39876728
|
T | C | 1 | a0001c0002t0002g0264 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1301+1260T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876728 | ||||||
| chr6:39876730
|
C | T | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 223 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1301+1262C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876730 | ||||||
| chr6:39876786
|
T | C | 1 | a0001c0002t0002g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1301+1318T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876786 | ||||||
| chr6:39876810
|
C | T | 10 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(7): Show | 10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1301+1342C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876810 | ||||||
| chr6:39876844
|
C | G | 8 | a0001c0005t0014g0175a0001c0006t0001g0040a0001c0006t0001g0152others(5): Show | 8 | HG00741.hp2 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302-1359C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876844 | ||||||
| chr6:39876887
|
G | A | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1302-1316G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876887 | ||||||
| chr6:39876942
|
T | C | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 226 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1302-1261T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876942 | ||||||
| chr6:39877022
|
A | C | 1 | a0001c0007t0013g0064 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1302-1181A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877022 | ||||||
| chr6:39877033
|
A | G | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1302-1170A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877033 | ||||||
| chr6:39877068
|
C | T | 1 | a0001c0002t0002g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1302-1135C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877068 | ||||||
| chr6:39877170
|
C | G | 1 | a0001c0002t0002g0261 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1302-1033C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877170 | ||||||
| chr6:39877769
|
G | A | 3 | a0001c0004t0003g0115a0001c0033t0001g0044a0017c0019t0003g0036 | 3 | HG02615.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1302-434G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877769 | ||||||
| chr6:39877802
|
G | T | 1 | a0001c0004t0031g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302-401G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877802 | ||||||
| chr6:39877855
|
G | A | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1302-348G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877855 | ||||||
| chr6:39878012
|
C | A | 1 | a0001c0045t0002g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1302-191C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39878012 | ||||||
| chr6:39878161
|
T | A | 3 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080 | 3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1302-42T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39878161 | ||||||
| chr6:39878326
|
C | T | 1 | a0001c0007t0012g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1360+65C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/24 | chr6 | 39878326 | ||||||
| chr6:39878333
|
C | G | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1361-71C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/24 | chr6 | 39878333 | ||||||
| chr6:39878361
|
A | G | 196 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(193): Show | 196 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1361-43A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/24 | chr6 | 39878361 | ||||||
| chr6:39878765
|
G | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0001g0259 | 3 | HG01175.hp2 HG01361.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1545+177G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878765 | ||||||
| chr6:39878799
|
G | C | 224 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(221): Show | 224 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1545+211G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878799 | ||||||
| chr6:39878914
|
G | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0234others(2): Show | 5 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-264G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878914 | ||||||
| chr6:39878940
|
A | G | 29 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0123others(26): Show | 29 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.1546-238A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878940 | ||||||
| chr6:39878959
|
C | T | 1 | a0001c0003t0003g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1546-219C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878959 | ||||||
| chr6:39879083
|
T | C | 3 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080 | 3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1546-95T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39879083 | ||||||
| chr6:39879503
|
G | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0072others(19): Show | 22 | HG00323.hp1 HG00735.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1845+26G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39879503 | ||||||
| chr6:39879696
|
A | C | 4 | a0001c0004t0003g0102a0001c0004t0003g0115a0001c0033t0001g0044others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+219A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39879696 | ||||||
| chr6:39879902
|
A | C | 19 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0002t0002g0107others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1845+425A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39879902 | ||||||
| chr6:39880018
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1845+541G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880018 | ||||||
| chr6:39880333
|
C | T | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+856C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880333 | ||||||
| chr6:39880402
|
C | T | 36 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0002t0002g0107others(33): Show | 36 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1845+925C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880402 | ||||||
| chr6:39880542
|
C | T | 1 | a0001c0003t0003g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1845+1065C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880542 | ||||||
| chr6:39880543
|
A | G | 228 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(225): Show | 228 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1845+1066A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880543 | ||||||
| chr6:39880645
|
TG | T | 36 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0002t0002g0107others(33): Show | 36 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1845+1169delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880645 | ||||||
| chr6:39880656
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1845+1179C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880656 | ||||||
| chr6:39880758
|
C | T | 10 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845+1281C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880758 | ||||||
| chr6:39880946
|
G | A | 8 | a0001c0005t0014g0175a0001c0006t0001g0040a0001c0006t0001g0152others(5): Show | 8 | HG00741.hp2 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1845+1469G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880946 | ||||||
| chr6:39881104
|
G | A | 4 | a0001c0002t0002g0145a0001c0002t0002g0156a0001c0002t0002g0250others(1): Show | 4 | HG00099.hp2 HG00642.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+1627G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881104 | ||||||
| chr6:39881239
|
AG | A | 145 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(142): Show | 145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1845+1763delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881239 | ||||||
| chr6:39881297
|
C | T | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1845+1820C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881297 | ||||||
| chr6:39881298
|
G | A | 11 | a0001c0004t0007g0237a0001c0007t0003g0058a0001c0007t0012g0078others(8): Show | 11 | HG02735.hp1 NA18747.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1845+1821G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881298 | ||||||
| chr6:39881393
|
T | G | 225 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(222): Show | 225 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1845+1916T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881393 | ||||||
| chr6:39881441
|
G | A | 32 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0123others(29): Show | 32 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1845+1964G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881441 | ||||||
| chr6:39881488
|
G | A | 1 | a0001c0022t0020g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1845+2011G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881488 | ||||||
| chr6:39881489
|
C | T | 1 | a0001c0009t0029g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1845+2012C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881489 | ||||||
| chr6:39881554
|
T | TA | 37 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0123others(34): Show | 37 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.1845+2082dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39881554 | |||||
| chr6:39881585
|
C | T | 5 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(2): Show | 5 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1845+2108C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881585 | ||||||
| chr6:39881645
|
G | A | 2 | a0001c0001t0001g0259a0001c0003t0003g0154 | 2 | HG02738.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1845+2168G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881645 | ||||||
| chr6:39881873
|
G | A | 1 | a0001c0005t0003g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1846-2089G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881873 | ||||||
| chr6:39882199
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0105a0001c0001t0001g0127others(4): Show | 7 | HG00323.hp1 HG01106.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1846-1763C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882199 | ||||||
| chr6:39882216
|
T | C | 2 | a0001c0004t0035g0126a0011c0029t0001g0177 | 2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1846-1746T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882216 | ||||||
| chr6:39882333
|
G | T | 9 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1846-1629G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882333 | ||||||
| chr6:39882393
|
A | C | 1 | a0001c0044t0022g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1846-1569A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882393 | ||||||
| chr6:39882497
|
T | C | 23 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(20): Show | 23 | HG01884.hp1 HG01891.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1846-1465T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882497 | ||||||
| chr6:39882522
|
T | C | 198 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(195): Show | 198 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1846-1440T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882522 | ||||||
| chr6:39882560
|
G | C | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(218): Show | 221 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.1846-1402G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882560 | ||||||
| chr6:39882702
|
C | T | 3 | a0001c0002t0002g0125a0001c0006t0001g0013a0001c0006t0001g0135 | 3 | HG01358.hp2 HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1846-1260C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882702 | ||||||
| chr6:39882703
|
GCACACAC others(3): Show |
G | 212 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 212 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1846-1253_1846-124 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39882703 | |||||
| chr6:39882719
|
GCACACAC others(1): Show |
G | 9 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1846-1236_1846-122 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39882719 | |||||
| chr6:39882732
|
C | T | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1846-1230C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882732 | ||||||
| chr6:39882798
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1846-1164C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882798 | ||||||
| chr6:39882852
|
G | T | 1 | a0001c0002t0002g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1846-1110G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882852 | ||||||
| chr6:39882867
|
G | C | 196 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(193): Show | 196 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1846-1095G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882867 | ||||||
| chr6:39882943
|
G | A | 20 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(17): Show | 20 | HG02083.hp2 HG02129.hp1 HG04184.hp2 others(17): Show |
intron_variant | MODIFIER | c.1846-1019G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882943 | ||||||
| chr6:39883028
|
G | A | 19 | a0001c0002t0002g0125a0001c0004t0003g0102a0001c0004t0031g0294others(16): Show | 19 | HG00741.hp2 HG01081.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1846-934G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883028 | ||||||
| chr6:39883089
|
T | C | 4 | a0001c0008t0005g0165a0001c0008t0005g0286a0001c0008t0024g0033others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1846-873T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883089 | ||||||
| chr6:39883184
|
CTT | C | 17 | a0001c0001t0001g0096a0001c0001t0001g0106a0001c0001t0001g0112others(14): Show | 17 | HG00621.hp2 HG02055.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1846-763_1846-762d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39883184 | |||||
| chr6:39883184
|
CTTT | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 217 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1846-764_1846-762d others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39883184 | |||||
| chr6:39883202
|
G | T | 3 | a0001c0009t0009g0162a0001c0014t0001g0029a0001c0014t0017g0266 | 3 | HG02055.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1846-760G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883202 | ||||||
| chr6:39883203
|
C | G | 1 | a0001c0003t0003g0290 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1846-759C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883203 | ||||||
| chr6:39883264
|
C | A | 3 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0026t0001g0280 | 3 | HG01884.hp1 HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1846-698C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883264 | ||||||
| chr6:39883502
|
C | T | 67 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0024others(64): Show | 67 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1846-460C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883502 | ||||||
| chr6:39883571
|
G | A | 4 | a0001c0013t0023g0169a0001c0013t0023g0170a0001c0026t0001g0280others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1846-391G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883571 | ||||||
| chr6:39883623
|
C | T | 2 | a0001c0007t0012g0078a0001c0007t0012g0079 | 2 | NA18747.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1846-339C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883623 | ||||||
| chr6:39883665
|
G | C | 239 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(236): Show | 239 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.1846-297G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883665 | ||||||
| chr6:39883685
|
A | G | 10 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(7): Show | 10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1846-277A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883685 | ||||||
| chr6:39883903
|
A | G | 115 | a0001c0002t0002g0007a0001c0002t0002g0018a0001c0002t0002g0019others(112): Show | 115 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1846-59A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883903 | ||||||
| chr6:39884261
|
T | C | 160 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(157): Show | 160 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1953+192T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884261 | ||||||
| chr6:39884287
|
G | A | 67 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0024others(64): Show | 67 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1953+218G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884287 | ||||||
| chr6:39884506
|
T | C | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1953+437T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884506 | ||||||
| chr6:39884618
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1953+549A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884618 | ||||||
| chr6:39884626
|
G | GCTGGGC | 11 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(8): Show | 11 | HG02109.hp2 NA18747.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1953+575_1953+580d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr6 | 39884626 | |||||
| chr6:39884626
|
GCTGGGC | G | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+575_1953+580d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr6 | 39884626 | |||||
| chr6:39884645
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1953+576C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884645 | ||||||
| chr6:39884662
|
A | G | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+593A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884662 | ||||||
| chr6:39884759
|
C | T | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1953+690C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884759 | ||||||
| chr6:39884802
|
T | C | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+733T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884802 | ||||||
| chr6:39884831
|
T | G | 1 | a0001c0022t0020g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1953+762T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884831 | ||||||
| chr6:39884857
|
G | A | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+788G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884857 | ||||||
| chr6:39884908
|
C | T | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+839C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884908 | ||||||
| chr6:39885074
|
A | G | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 186 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1953+1005A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885074 | ||||||
| chr6:39885144
|
C | T | 10 | a0001c0001t0001g0034a0001c0001t0001g0071a0001c0001t0001g0086others(7): Show | 10 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1953+1075C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885144 | ||||||
| chr6:39885174
|
T | C | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1953+1105T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885174 | ||||||
| chr6:39885177
|
C | T | 1 | a0001c0004t0004g0037 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1953+1108C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885177 | ||||||
| chr6:39885188
|
T | A | 28 | a0001c0002t0002g0125a0001c0005t0011g0030a0001c0005t0011g0042others(25): Show | 28 | HG00741.hp2 HG01081.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1953+1119T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885188 | ||||||
| chr6:39885189
|
G | A | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+1120G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885189 | ||||||
| chr6:39885189
|
G | T | 6 | a0001c0002t0002g0132a0001c0002t0002g0133a0001c0002t0002g0146others(3): Show | 6 | HG01109.hp1 HG01169.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1953+1120G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885189 | ||||||
| chr6:39885346
|
T | TA | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+1277_1953+127 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885346 | ||||||
| chr6:39885363
|
G | A | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+1294G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885363 | ||||||
| chr6:39885382
|
TG | T | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+1317delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr6 | 39885382 | |||||
| chr6:39885413
|
C | T | 25 | a0001c0004t0003g0102a0001c0004t0004g0037a0001c0004t0004g0046others(22): Show | 25 | HG02083.hp2 HG02129.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1953+1344C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885413 | ||||||
| chr6:39885414
|
A | G | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+1345A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885414 | ||||||
| chr6:39885588
|
G | A | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+1519G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885588 | ||||||
| chr6:39885655
|
T | G | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1953+1586T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885655 | ||||||
| chr6:39885666
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1953+1597G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885666 | ||||||
| chr6:39885667
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1953+1598C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885667 | ||||||
| chr6:39885778
|
T | C | 1 | a0001c0004t0007g0237 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1954-1708T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885778 | ||||||
| chr6:39885795
|
T | A | 161 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(158): Show | 161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1954-1691T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885795 | ||||||
| chr6:39885853
|
A | T | 10 | a0001c0001t0001g0034a0001c0001t0001g0071a0001c0001t0001g0086others(7): Show | 10 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1954-1633A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885853 | ||||||
| chr6:39885868
|
A | T | 6 | a0001c0002t0002g0026a0001c0002t0002g0038a0001c0002t0002g0278others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1954-1618A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885868 | ||||||
| chr6:39885874
|
G | A | 25 | a0001c0004t0003g0102a0001c0004t0004g0037a0001c0004t0004g0046others(22): Show | 25 | HG02083.hp2 HG02129.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1954-1612G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885874 | ||||||
| chr6:39885879
|
G | A | 4 | a0001c0004t0021g0060a0001c0004t0021g0100a0001c0004t0031g0294others(1): Show | 4 | HG02451.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954-1607G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885879 | ||||||
| chr6:39886022
|
A | G | 1 | a0013c0038t0009g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1954-1464A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886022 | ||||||
| chr6:39886170
|
C | T | 4 | a0001c0005t0004g0063a0001c0005t0004g0081a0001c0005t0004g0212others(1): Show | 4 | NA18952.hp2 NA19011.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954-1316C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886170 | ||||||
| chr6:39886186
|
G | T | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 186 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1954-1300G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886186 | ||||||
| chr6:39886187
|
G | A | 1 | a0001c0003t0003g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1954-1299G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886187 | ||||||
| chr6:39886202
|
C | T | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1954-1284C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886202 | ||||||
| chr6:39886301
|
T | C | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 186 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1954-1185T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886301 | ||||||
| chr6:39886469
|
G | A | 1 | a0001c0002t0002g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1954-1017G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886469 | ||||||
| chr6:39886649
|
A | G | 241 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(238): Show | 241 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1954-837A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886649 | ||||||
| chr6:39886884
|
C | T | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1954-602C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886884 | ||||||
| chr6:39886885
|
G | A | 5 | a0001c0002t0002g0026a0001c0002t0002g0038a0001c0002t0002g0278others(2): Show | 5 | HG02451.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1954-601G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886885 | ||||||
| chr6:39887125
|
G | T | 195 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(192): Show | 195 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1954-361G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887125 | ||||||
| chr6:39887224
|
A | C | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 186 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1954-262A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887224 | ||||||
| chr6:39887240
|
T | TA | 10 | a0001c0007t0003g0058a0001c0007t0012g0078a0001c0007t0012g0079others(7): Show | 10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1954-238dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr6 | 39887240 | |||||
| chr6:39887243
|
A | C | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1954-243A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887243 | ||||||
| chr6:39887315
|
G | A | 4 | a0001c0004t0021g0060a0001c0004t0021g0100a0001c0004t0031g0294others(1): Show | 4 | HG02451.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954-171G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887315 | ||||||
| chr6:39887336
|
T | G | 200 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(197): Show | 200 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1954-150T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887336 | ||||||
| chr6:39887428
|
G | A | 1 | a0001c0004t0003g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1954-58G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887428 | ||||||
| chr6:39887651
|
C | T | 149 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.2060+59C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39887651 | ||||||
| chr6:39887714
|
C | CTGGA | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 148 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.2060+123_2060+126d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr6 | 39887714 | |||||
| chr6:39887810
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2060+218C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39887810 | ||||||
| chr6:39887953
|
G | A | 1 | a0001c0002t0002g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2060+361G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39887953 | ||||||
| chr6:39888002
|
A | G | 1 | a0001c0008t0005g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2060+410A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39888002 | ||||||
| chr6:39888172
|
C | T | 7 | a0001c0004t0004g0205a0001c0004t0006g0074a0001c0004t0006g0089others(4): Show | 7 | NA18939.hp2 NA18945.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.2061-507C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39888172 | ||||||
| chr6:39888380
|
G | T | 67 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0024others(64): Show | 67 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2061-299G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39888380 | ||||||
| chr6:39888611
|
C | T | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2061-68C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39888611 | ||||||
| chr6:39888775
|
C | T | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2145+12C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39888775 | ||||||
| chr6:39888804
|
G | A | 4 | a0001c0008t0005g0165a0001c0008t0005g0286a0001c0008t0024g0033others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2145+41G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39888804 | ||||||
| chr6:39888863
|
A | G | 1 | a0001c0002t0002g0264 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2145+100A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39888863 | ||||||
| chr6:39888913
|
A | G | 151 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.2145+150A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39888913 | ||||||
| chr6:39889092
|
T | A | 54 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.2145+329T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889092 | ||||||
| chr6:39889146
|
A | G | 1 | a0001c0012t0002g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2145+383A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889146 | ||||||
| chr6:39889210
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2145+447G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889210 | ||||||
| chr6:39889534
|
A | G | 4 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(1): Show | 4 | HG02083.hp2 NA18956.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.2145+771A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889534 | ||||||
| chr6:39889537
|
C | T | 1 | a0001c0002t0002g0107 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2145+774C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889537 | ||||||
| chr6:39889545
|
TA | T | 10 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080others(7): Show | 10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.2145+783delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889545 | ||||||
| chr6:39889550
|
A | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.2145+787A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889550 | ||||||
| chr6:39889633
|
G | A | 115 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 115 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2145+870G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889633 | ||||||
| chr6:39889710
|
G | A | 149 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.2145+947G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889710 | ||||||
| chr6:39889746
|
A | G | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2145+983A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889746 | ||||||
| chr6:39889819
|
C | T | 16 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0193others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.2145+1056C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889819 | ||||||
| chr6:39890125
|
C | CA | 150 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2146-1207dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr6 | 39890125 | |||||
| chr6:39890155
|
C | T | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 217 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2146-1186C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890155 | ||||||
| chr6:39890325
|
C | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2146-1016C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890325 | ||||||
| chr6:39890508
|
T | C | 1 | a0001c0005t0004g0063 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2146-833T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890508 | ||||||
| chr6:39890536
|
G | C | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2146-805G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890536 | ||||||
| chr6:39890688
|
A | C | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2146-653A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890688 | ||||||
| chr6:39890718
|
T | C | 5 | a0001c0004t0021g0060a0001c0004t0021g0100a0001c0004t0031g0294others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2146-623T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890718 | ||||||
| chr6:39890965
|
A | C | 1 | a0001c0001t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2146-376A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890965 | ||||||
| chr6:39890991
|
C | T | 3 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080 | 3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2146-350C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890991 | ||||||
| chr6:39891027
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0017g0267 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2146-314C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39891027 | ||||||
| chr6:39891090
|
T | TA | 150 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2146-236dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr6 | 39891090 | |||||
| chr6:39891090
|
TA | T | 12 | a0001c0002t0002g0018a0001c0002t0002g0247a0001c0004t0007g0237others(9): Show | 12 | HG02027.hp2 HG02735.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.2146-236delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr6 | 39891090 | |||||
| chr6:39891315
|
G | A | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2146-26G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39891315 | ||||||
| chr6:39891326
|
G | A | 45 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2146-15G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39891326 | ||||||
| chr6:39891476
|
AGCAGGTG others(17): Show |
A | 2 | a0001c0003t0039g0090a0009c0041t0014g0147 | 2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2252+40_2252+63del others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr6 | 39891476 | |||||
| chr6:39891611
|
G | T | 53 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(50): Show | 53 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.2253-23G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 18/24 | chr6 | 39891611 | ||||||
| chr6:39891745
|
G | A | 3 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080 | 3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2341+23G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891745 | ||||||
| chr6:39891865
|
C | G | 10 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080others(7): Show | 10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.2341+143C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891865 | ||||||
| chr6:39891891
|
T | C | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2341+169T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891891 | ||||||
| chr6:39891921
|
C | A | 1 | a0001c0004t0004g0070 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2341+199C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891921 | ||||||
| chr6:39891972
|
G | A | 3 | a0001c0004t0021g0060a0001c0004t0021g0100a0001c0022t0020g0047 | 3 | HG02451.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2341+250G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891972 | ||||||
| chr6:39892074
|
T | C | 56 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2341+352T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892074 | ||||||
| chr6:39892108
|
C | T | 10 | a0001c0007t0012g0078a0001c0007t0012g0079a0001c0007t0012g0080others(7): Show | 10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.2341+386C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892108 | ||||||
| chr6:39892109
|
T | C | 151 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.2341+387T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892109 | ||||||
| chr6:39892143
|
A | G | 2 | a0001c0017t0018g0052a0007c0018t0018g0053 | 2 | NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2341+421A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892143 | ||||||
| chr6:39892154
|
G | T | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2341+432G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892154 | ||||||
| chr6:39892173
|
G | A | 1 | a0001c0003t0016g0284 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2341+451G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892173 | ||||||
| chr6:39892254
|
C | T | 115 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 115 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2341+532C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892254 | ||||||
| chr6:39892294
|
A | G | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2341+572A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892294 | ||||||
| chr6:39892305
|
A | G | 35 | a0001c0004t0003g0102a0001c0004t0004g0037a0001c0004t0004g0046others(32): Show | 35 | HG01884.hp2 HG02055.hp2 HG02083.hp2 others(32): Show |
intron_variant | MODIFIER | c.2341+583A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892305 | ||||||
| chr6:39892317
|
C | T | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.2341+595C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892317 | ||||||
| chr6:39892335
|
A | C | 61 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0024others(58): Show | 61 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2341+613A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892335 | ||||||
| chr6:39892377
|
G | A | 74 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2341+655G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892377 | ||||||
| chr6:39892990
|
A | G | 1 | a0001c0007t0013g0082 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2341+1268A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892990 | ||||||
| chr6:39893078
|
C | T | 1 | a0001c0008t0005g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2341+1356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893078 | ||||||
| chr6:39893181
|
G | A | 63 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0024others(60): Show | 63 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.2341+1459G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893181 | ||||||
| chr6:39893281
|
C | T | 1 | a0001c0003t0016g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2341+1559C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893281 | ||||||
| chr6:39893291
|
C | A | 1 | a0001c0005t0006g0197 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2341+1569C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893291 | ||||||
| chr6:39893358
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0275 | 2 | NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2341+1636A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893358 | ||||||
| chr6:39893366
|
A | C | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2341+1644A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893366 | ||||||
| chr6:39893399
|
T | C | 1 | a0001c0012t0002g0219 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2341+1677T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893399 | ||||||
| chr6:39893402
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0001g0259 | 3 | HG01175.hp2 HG01361.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2341+1680C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893402 | ||||||
| chr6:39893450
|
G | A | 18 | a0001c0004t0012g0098a0001c0007t0012g0078a0001c0007t0012g0079others(15): Show | 18 | HG01361.hp2 HG02109.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2341+1728G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893450 | ||||||
| chr6:39893553
|
T | C | 29 | a0001c0004t0003g0102a0001c0004t0012g0098a0001c0007t0012g0078others(26): Show | 29 | HG01361.hp2 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.2341+1831T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893553 | ||||||
| chr6:39893625
|
G | A | 3 | a0001c0006t0020g0285a0001c0006t0027g0188a0001c0022t0020g0047 | 3 | HG02486.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2341+1903G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893625 | ||||||
| chr6:39893642
|
T | A | 1 | a0001c0002t0002g0144 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2341+1920T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893642 | ||||||
| chr6:39893743
|
G | A | 28 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(25): Show | 28 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.2341+2021G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893743 | ||||||
| chr6:39893819
|
G | A | 48 | a0001c0002t0002g0007a0001c0002t0002g0018a0001c0002t0002g0021others(45): Show | 48 | HG00099.hp2 HG00642.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2341+2097G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893819 | ||||||
| chr6:39893904
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0010g0269 | 2 | HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2341+2182G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893904 | ||||||
| chr6:39894016
|
C | T | 62 | a0001c0002t0002g0184a0001c0003t0003g0002a0001c0003t0003g0008others(59): Show | 62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.2341+2294C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894016 | ||||||
| chr6:39894030
|
ATTC | A | 6 | a0001c0009t0009g0111a0001c0009t0009g0128a0001c0009t0009g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2341+2314_2341+231 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39894030 | |||||
| chr6:39894203
|
G | A | 1 | a0001c0005t0004g0049 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2341+2481G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894203 | ||||||
| chr6:39894297
|
C | T | 1 | a0018c0047t0001g0066 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2342-2515C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894297 | ||||||
| chr6:39894406
|
G | C | 3 | a0004c0020t0001g0277a0004c0030t0001g0192a0006c0021t0001g0297 | 3 | HG01081.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2342-2406G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894406 | ||||||
| chr6:39894473
|
A | C | 1 | a0001c0001t0033g0226 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2342-2339A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894473 | ||||||
| chr6:39894501
|
C | A | 5 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(2): Show | 5 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2342-2311C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894501 | ||||||
| chr6:39894596
|
G | A | 1 | a0001c0001t0017g0267 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2342-2216G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894596 | ||||||
| chr6:39894596
|
G | C | 64 | a0001c0002t0002g0184a0001c0003t0003g0002a0001c0003t0003g0008others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-2216G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894596 | ||||||
| chr6:39894596
|
G | T | 1 | a0001c0003t0003g0103 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2342-2216G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894596 | ||||||
| chr6:39894604
|
A | G | 3 | a0001c0003t0014g0085a0001c0003t0014g0210a0001c0005t0014g0175 | 3 | HG02818.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2342-2208A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894604 | ||||||
| chr6:39894623
|
T | A | 65 | a0001c0002t0002g0184a0001c0003t0003g0002a0001c0003t0003g0008others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2342-2189T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894623 | ||||||
| chr6:39894630
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2342-2182T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894630 | ||||||
| chr6:39894650
|
C | T | 65 | a0001c0002t0002g0184a0001c0003t0003g0002a0001c0003t0003g0008others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2342-2162C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894650 | ||||||
| chr6:39894685
|
ATCTTGGC others(17): Show |
A | 5 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(2): Show | 5 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2342-2124_2342-210 others(28): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39894685 | |||||
| chr6:39894819
|
A | G | 1 | a0001c0006t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2342-1993A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894819 | ||||||
| chr6:39895158
|
T | C | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1654T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895158 | ||||||
| chr6:39895218
|
C | CTTTATTT others(5): Show |
2 | a0001c0005t0004g0063a0001c0005t0004g0212 | 2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2342-1586_2342-158 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895218 | |||||
| chr6:39895218
|
CTTTATTT others(5): Show |
C | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1585_2342-157 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895218 | |||||
| chr6:39895227
|
C | CTTACTTA others(5): Show |
11 | a0001c0001t0001g0034a0001c0001t0001g0071a0001c0001t0001g0086others(8): Show | 11 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2342-1582_2342-158 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | |||||
| chr6:39895227
|
C | CTTACTTA others(9): Show |
2 | a0001c0001t0001g0012a0001c0006t0001g0295 | 2 | HG01993.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2342-1582_2342-158 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | |||||
| chr6:39895227
|
C | CTTATTTA others(1): Show |
26 | a0001c0001t0001g0118a0001c0001t0001g0240a0001c0001t0008g0215others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.2342-1566_2342-155 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | |||||
| chr6:39895227
|
C | CTTATTTA others(5): Show |
66 | a0001c0001t0001g0010a0001c0001t0001g0067a0001c0001t0001g0069others(63): Show | 66 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.2342-1570_2342-155 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | |||||
| chr6:39895227
|
C | CTTATTTA others(9): Show |
43 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0039others(40): Show | 43 | HG00323.hp1 HG00642.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.2342-1574_2342-155 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | |||||
| chr6:39895227
|
C | CTTATTTA others(13): Show |
15 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0065others(12): Show | 15 | HG01891.hp1 HG02559.hp1 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.2342-1578_2342-155 others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | |||||
| chr6:39895227
|
C | CTTATTTA others(17): Show |
1 | a0001c0001t0001g0275 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2342-1582_2342-155 others(28): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | |||||
| chr6:39895227
|
C | T | 2 | a0001c0005t0004g0063a0001c0005t0004g0212 | 2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2342-1585C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895227 | ||||||
| chr6:39895259
|
G | A | 1 | a0001c0003t0014g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2342-1553G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895259 | ||||||
| chr6:39895345
|
C | T | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2342-1467C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895345 | ||||||
| chr6:39895435
|
C | T | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1377C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895435 | ||||||
| chr6:39895436
|
G | A | 1 | a0001c0001t0008g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2342-1376G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895436 | ||||||
| chr6:39895441
|
A | G | 243 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(240): Show | 243 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.2342-1371A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895441 | ||||||
| chr6:39895451
|
T | G | 203 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(200): Show | 203 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.2342-1361T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895451 | ||||||
| chr6:39895456
|
G | C | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1356G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895456 | ||||||
| chr6:39895478
|
T | C | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1334T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895478 | ||||||
| chr6:39895519
|
T | A | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1293T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895519 | ||||||
| chr6:39895576
|
G | A | 2 | a0001c0001t0019g0050a0001c0001t0019g0121 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2342-1236G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895576 | ||||||
| chr6:39895692
|
C | T | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1120C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895692 | ||||||
| chr6:39895703
|
G | T | 3 | a0001c0003t0003g0035a0001c0003t0003g0056a0001c0003t0003g0068 | 3 | HG01975.hp1 NA18940.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2342-1109G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895703 | ||||||
| chr6:39895791
|
C | T | 1 | a0001c0004t0004g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2342-1021C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895791 | ||||||
| chr6:39895828
|
A | C | 11 | a0001c0004t0012g0098a0001c0007t0012g0078a0001c0007t0012g0079others(8): Show | 11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.2342-984A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895828 | ||||||
| chr6:39895831
|
T | C | 6 | a0001c0003t0003g0059a0001c0003t0003g0154a0001c0003t0003g0179others(3): Show | 6 | HG00423.hp1 HG00621.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2342-981T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895831 | ||||||
| chr6:39895852
|
C | CCA | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-960_2342-959i others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895852 | ||||||
| chr6:39895853
|
A | T | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-959A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895853 | ||||||
| chr6:39895857
|
A | C | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-955A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895857 | ||||||
| chr6:39895858
|
G | C | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-954G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895858 | ||||||
| chr6:39895859
|
A | C | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-953A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895859 | ||||||
| chr6:39895860
|
G | C | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-952G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895860 | ||||||
| chr6:39895863
|
T | A | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-949T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895863 | ||||||
| chr6:39895866
|
G | C | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-946G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895866 | ||||||
| chr6:39895867
|
G | T | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-945G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895867 | ||||||
| chr6:39895868
|
G | C | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-944G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895868 | ||||||
| chr6:39895869
|
G | T | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-943G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895869 | ||||||
| chr6:39895872
|
AAT | A | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-939_2342-938d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895872 | ||||||
| chr6:39895875
|
G | T | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-937G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895875 | ||||||
| chr6:39895959
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0109 | 3 | HG02015.hp1 NA18966.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2342-853C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895959 | ||||||
| chr6:39896018
|
T | G | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-794T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896018 | ||||||
| chr6:39896038
|
A | ATT | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-767_2342-766d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39896038 | |||||
| chr6:39896062
|
A | G | 27 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(24): Show | 27 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2342-750A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896062 | ||||||
| chr6:39896071
|
A | T | 1 | a0001c0009t0029g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2342-741A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896071 | ||||||
| chr6:39896082
|
A | C | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-730A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896082 | ||||||
| chr6:39896087
|
C | T | 1 | a0001c0007t0015g0057 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2342-725C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896087 | ||||||
| chr6:39896182
|
A | G | 2 | a0001c0013t0023g0169a0001c0013t0023g0170 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2342-630A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896182 | ||||||
| chr6:39896194
|
T | TTTTTTTC | 151 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.2342-598_2342-592d others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39896194 | |||||
| chr6:39896194
|
T | TTTTTTTT others(1): Show |
26 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.2342-612_2342-611i others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39896194 | |||||
| chr6:39896333
|
T | G | 202 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(199): Show | 202 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.2342-479T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896333 | ||||||
| chr6:39896396
|
G | T | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2342-416G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896396 | ||||||
| chr6:39896406
|
G | A | 71 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(68): Show | 71 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2342-406G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896406 | ||||||
| chr6:39896424
|
G | A | 3 | a0001c0006t0001g0295a0001c0014t0001g0029a0001c0014t0017g0266 | 3 | HG02280.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2342-388G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896424 | ||||||
| chr6:39896449
|
T | C | 243 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(240): Show | 243 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.2342-363T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896449 | ||||||
| chr6:39896517
|
T | G | 3 | a0002c0010t0002g0095a0002c0010t0002g0236a0002c0010t0002g0255 | 3 | HG02015.hp2 HG02027.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2342-295T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896517 | ||||||
| chr6:39896536
|
A | G | 1 | a0001c0003t0003g0129 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2342-276A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896536 | ||||||
| chr6:39896740
|
T | C | 39 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(36): Show | 39 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.2342-72T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896740 | ||||||
| chr6:39896781
|
G | A | 64 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-31G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896781 | ||||||
| chr6:39896802
|
C | T | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2342-10C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896802 | ||||||
| chr6:39896988
|
C | T | 4 | a0001c0005t0011g0030a0001c0005t0011g0042a0001c0005t0011g0092others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2510+8C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 20/24 | chr6 | 39896988 | ||||||
| chr6:39897090
|
TC | T | 3 | a0001c0004t0021g0060a0001c0004t0021g0100a0001c0004t0031g0294 | 3 | HG02451.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2511-84delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 20/24 | chr6 | 39897090 | ||||||
| chr6:39897423
|
A | C | 1 | a0001c0003t0003g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2618+141A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39897423 | ||||||
| chr6:39897596
|
A | C | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2618+314A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39897596 | ||||||
| chr6:39897743
|
G | GT | 11 | a0001c0004t0012g0098a0001c0007t0012g0078a0001c0007t0012g0079others(8): Show | 11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.2618+468dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr6 | 39897743 | |||||
| chr6:39897865
|
T | C | 3 | a0001c0004t0021g0060a0001c0004t0021g0100a0001c0004t0031g0294 | 3 | HG02451.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2618+583T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39897865 | ||||||
| chr6:39897894
|
G | C | 13 | a0001c0002t0002g0045a0001c0002t0002g0097a0001c0002t0002g0180others(10): Show | 13 | HG02015.hp2 HG02027.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2618+612G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39897894 | ||||||
| chr6:39898168
|
G | A | 27 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(24): Show | 27 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2619-709G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898168 | ||||||
| chr6:39898183
|
A | T | 1 | a0001c0009t0009g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2619-694A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898183 | ||||||
| chr6:39898234
|
GCAAT | G | 4 | a0001c0004t0012g0098a0001c0007t0012g0078a0001c0007t0012g0079others(1): Show | 4 | NA18747.hp1 NA18954.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.2619-640_2619-637d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr6 | 39898234 | |||||
| chr6:39898347
|
G | A | 231 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(228): Show | 231 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.2619-530G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898347 | ||||||
| chr6:39898416
|
A | AGCATCTG others(14): Show |
1 | a0001c0003t0003g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2619-460_2619-440d others(23): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr6 | 39898416 | |||||
| chr6:39898494
|
G | T | 1 | a0001c0025t0034g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2619-383G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898494 | ||||||
| chr6:39898514
|
G | A | 130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(127): Show | 130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.2619-363G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898514 | ||||||
| chr6:39898580
|
T | C | 1 | a0001c0012t0002g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2619-297T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898580 | ||||||
| chr6:39898993
|
C | T | 27 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(24): Show | 27 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2679+56C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39898993 | ||||||
| chr6:39898994
|
G | A | 1 | a0001c0003t0003g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2679+57G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39898994 | ||||||
| chr6:39899029
|
A | AACAATGG others(2): Show |
232 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(229): Show | 232 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2679+100_2679+101i others(11): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr6 | 39899029 | |||||
| chr6:39899132
|
C | T | 3 | a0004c0020t0001g0277a0004c0030t0001g0192a0006c0021t0001g0297 | 3 | HG01081.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2679+195C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899132 | ||||||
| chr6:39899229
|
A | G | 3 | a0001c0001t0010g0015a0001c0001t0010g0017a0001c0001t0010g0084 | 3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2679+292A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899229 | ||||||
| chr6:39899243
|
T | C | 3 | a0001c0004t0021g0060a0001c0004t0021g0100a0001c0004t0031g0294 | 3 | HG02451.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2679+306T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899243 | ||||||
| chr6:39899271
|
G | A | 26 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.2679+334G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899271 | ||||||
| chr6:39899290
|
G | C | 11 | a0001c0004t0012g0098a0001c0007t0012g0078a0001c0007t0012g0079others(8): Show | 11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.2679+353G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899290 | ||||||
| chr6:39899347
|
G | A | 11 | a0001c0004t0012g0098a0001c0007t0012g0078a0001c0007t0012g0079others(8): Show | 11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.2679+410G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899347 | ||||||
| chr6:39899391
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2679+454C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899391 | ||||||
| chr6:39899399
|
A | G | 5 | a0001c0006t0001g0040a0001c0006t0001g0158a0001c0006t0020g0285others(2): Show | 5 | HG00741.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2679+462A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899399 | ||||||
| chr6:39899674
|
C | T | 1 | a0001c0002t0002g0238 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2680-403C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899674 | ||||||
| chr6:39899949
|
GA | G | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-127delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899949 | ||||||
| chr6:39899953
|
T | A | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-124T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899953 | ||||||
| chr6:39899954
|
GC | G | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-122delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899954 | ||||||
| chr6:39899960
|
T | A | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-117T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899960 | ||||||
| chr6:39899961
|
G | A | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-116G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899961 | ||||||
| chr6:39899962
|
T | C | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-115T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899962 | ||||||
| chr6:39899963
|
T | A | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-114T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899963 | ||||||
| chr6:39899967
|
T | TG | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-110_2680-109i others(3): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899967 | ||||||
| chr6:39899969
|
T | A | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-108T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899969 | ||||||
| chr6:39899971
|
C | CT | 50 | a0001c0003t0003g0002a0001c0003t0003g0008a0001c0003t0003g0014others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-106_2680-105i others(3): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899971 | ||||||
| chr6:39900021
|
G | C | 3 | a0001c0007t0013g0064a0001c0007t0013g0207a0001c0007t0013g0246 | 3 | NA18945.hp1 NA18956.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2680-56G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39900021 | ||||||
| chr6:39900027
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2680-50G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39900027 | ||||||
| chr6:39900052
|
G | A | 1 | a0001c0006t0001g0013 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2680-25G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39900052 | ||||||
| chr6:39900260
|
G | A | 26 | a0001c0004t0004g0037a0001c0004t0004g0046a0001c0004t0004g0051others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.2811+52G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900260 | ||||||
| chr6:39900298
|
G | A | 7 | a0001c0003t0003g0035a0001c0003t0003g0056a0001c0003t0003g0068others(4): Show | 7 | HG00438.hp1 HG01975.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2811+90G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900298 | ||||||
| chr6:39900305
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2811+97C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900305 | ||||||
| chr6:39900321
|
T | C | 2 | a0001c0036t0022g0167a0001c0044t0022g0114 | 2 | HG01361.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2811+113T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900321 | ||||||
| chr6:39900547
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2811+339T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900547 | ||||||
| chr6:39900598
|
A | T | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2811+390A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900598 | ||||||
| chr6:39900600
|
G | T | 1 | a0001c0046t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2811+392G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900600 | ||||||
| chr6:39900642
|
G | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0231 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2811+434G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900642 | ||||||
| chr6:39900698
|
T | A | 1 | a0011c0029t0001g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2811+490T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900698 | ||||||
| chr6:39900746
|
CT | C | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(196): Show | 199 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.2811+542delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr6 | 39900746 | |||||
| chr6:39900877
|
C | A | 3 | a0001c0001t0001g0112a0003c0011t0001g0003a0003c0011t0001g0006 | 3 | HG02970.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2812-425C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900877 | ||||||
| chr6:39900988
|
T | C | 9 | a0001c0008t0005g0025a0001c0008t0005g0101a0001c0008t0005g0165others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2812-314T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900988 | ||||||
| chr6:39901099
|
C | A | 7 | a0001c0003t0003g0014a0001c0003t0003g0059a0001c0003t0003g0154others(4): Show | 7 | HG00423.hp1 HG00621.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.2812-203C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39901099 | ||||||
| chr6:39901290
|
G | C | 201 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(198): Show | 201 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.2812-12G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39901290 | ||||||
| chr6:39901805
|
G | A | 1 | a0001c0008t0005g0166 | 1 | HG02109.hp1 | splice_region_variant&intron_variant | LOW | c.2983-8G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 24/24 | chr6 | 39901805 |