Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 201562 |
|---|---|
| ensemblid | ENSG00000206527.10 |
| hgncid | 9640 |
| symbol | HACD2 |
| name | 3-hydroxyacyl-CoA dehydratase 2 |
| refseq_nuc | NM_198402.5 |
| refseq_prot | NP_940684.1 |
| ensembl_nuc | ENST00000383657.10 |
| ensembl_prot | ENSP00000373153.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 123491554 |
| end | 123585053 |
| strand | - |
| ver | v1.2 |
| region | chr3:123491554-123585053 |
| region5000 | chr3:123486554-123590053 |
| regionname0 | HACD2_chr3_123491554_123585053 |
| regionname5000 | HACD2_chr3_123486554_123590053 |
| 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 | 254 | 349 | 88 | 60 | 151 | 12 | 36 | 119 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0002 | 0/0 | 254 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 765 | 152 | 43 | 32 | 47 | 7 | 21 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| c0002 | 0/0 | 765 | 102 | 17 | 14 | 65 | 1 | 5 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| c0003 | 0/0 | 765 | 94 | 27 | 14 | 39 | 4 | 10 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| c0004 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| c0005 | 0/0 | 765 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3361 | 87 | 5 | 15 | 54 | 5 | 8 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0002 | 0/0 | 3361 | 64 | 9 | 9 | 36 | 2 | 8 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0003 | 0/0 | 3361 | 61 | 14 | 5 | 38 | 0 | 4 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0004 | 0/1 | 3361 | 39 | 0 | 13 | 10 | 3 | 12 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0005 | 0/0 | 3361 | 26 | 15 | 6 | 5 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0006 | 1/0 | 3361 | 24 | 20 | 3 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0007 | 0/0 | 3361 | 8 | 0 | 5 | 1 | 1 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0008 | 0/0 | 3361 | 7 | 6 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0009 | 0/0 | 3361 | 4 | 0 | 0 | 4 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0010 | 0/0 | 3361 | 4 | 4 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0011 | 0/0 | 3361 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0012 | 0/0 | 3361 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0013 | 0/0 | 3361 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0014 | 0/0 | 3361 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0015 | 0/0 | 3361 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0016 | 0/0 | 3361 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0017 | 0/0 | 3361 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0018 | 0/0 | 3361 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0019 | 0/0 | 3361 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0020 | 0/0 | 3361 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0021 | 0/0 | 3361 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0022 | 0/0 | 3361 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0023 | 0/0 | 3361 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0024 | 0/0 | 3361 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0025 | 0/0 | 3361 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0026 | 0/0 | 3361 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0027 | 0/0 | 3361 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0028 | 0/0 | 3307 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0029 | 0/0 | 3361 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0030 | 0/0 | 3361 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| t0031 | 0/0 | 3361 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 765 | 152 | 43 | 32 | 47 | 7 | 21 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002 | 0/0 | 765 | 102 | 17 | 14 | 65 | 1 | 5 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003 | 0/0 | 765 | 94 | 27 | 14 | 39 | 4 | 10 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0004 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0002c0005 | 0/0 | 765 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4125 | 11 | 5 | 5 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0002 | 0/0 | 4125 | 63 | 9 | 9 | 36 | 2 | 7 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0003 | 0/0 | 4125 | 2 | 0 | 0 | 1 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0004 | 0/1 | 4125 | 33 | 0 | 12 | 5 | 3 | 12 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0005 | 0/0 | 4125 | 6 | 2 | 3 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0006 | 1/0 | 4125 | 24 | 20 | 3 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0009 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0013 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0015 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0018 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0019 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0025 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0027 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0028 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0029 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0030 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0001t0031 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0001 | 0/0 | 4125 | 65 | 0 | 7 | 53 | 1 | 4 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0002 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0003 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0004 | 0/0 | 4125 | 6 | 0 | 1 | 5 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0005 | 0/0 | 4125 | 17 | 10 | 3 | 4 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0008 | 0/0 | 4125 | 7 | 6 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0009 | 0/0 | 4125 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0020 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0022 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0002t0023 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0001 | 0/0 | 4125 | 10 | 0 | 3 | 0 | 3 | 4 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0003 | 0/0 | 4125 | 58 | 13 | 5 | 37 | 0 | 3 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0005 | 0/0 | 4125 | 3 | 3 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0007 | 0/0 | 4125 | 8 | 0 | 5 | 1 | 1 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0009 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0010 | 0/0 | 4125 | 4 | 4 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0011 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0012 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0014 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0016 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0021 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0024 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0003t0026 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0001c0004t0017 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| a0002c0005t0001 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | copy fasta | chr3 | 123486554 | 123590053 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0009g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0013g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0013g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0015g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0018g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0019g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0025g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0027g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0028g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0029g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0030g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0031g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0009g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0020g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0022g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0023g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0010g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0010g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0010g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0010g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0011g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0011g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0012g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0012g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0014g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0014g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0016g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0021g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0024g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0026g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0004t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0002c0005t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0007 | g0306 | EUR | GBR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0204 | EUR | GBR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0319 | EUR | GBR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0181 | EUR | GBR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0118 | EUR | FIN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0328 | EUR | FIN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00544 | hp2 | a0001 | c0003 | t0003 | g0266 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0062 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0064 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00642 | hp2 | a0001 | c0003 | t0007 | g0311 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0067 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00735 | hp1 | a0001 | c0003 | t0007 | g0305 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00735 | hp2 | a0001 | c0002 | t0008 | g0013 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0199 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0258 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0098 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01255 | hp2 | a0001 | c0003 | t0007 | g0308 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01261 | hp2 | a0001 | c0003 | t0007 | g0307 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01346 | hp1 | a0001 | c0003 | t0007 | g0310 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0113 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0187 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01433 | hp2 | a0001 | c0002 | t0005 | g0094 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01515 | hp1 | a0001 | c0001 | t0031 | g0342 | EUR | IBS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0182 | EUR | IBS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0178 | EUR | IBS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0314 | EUR | IBS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01884 | hp1 | a0001 | c0003 | t0012 | g0303 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01928 | hp2 | a0001 | c0003 | t0026 | g0261 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0279 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0317 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01993 | hp1 | a0001 | c0003 | t0003 | g0265 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01993 | hp2 | a0001 | c0002 | t0020 | g0056 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0264 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02004 | hp2 | a0001 | c0002 | t0023 | g0058 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02055 | hp1 | a0001 | c0003 | t0014 | g0299 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0289 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0274 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0263 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02129 | hp1 | a0001 | c0003 | t0007 | g0312 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0270 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0294 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02145 | hp2 | a0001 | c0003 | t0003 | g0313 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CDX | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | CDX | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0244 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0302 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02258 | hp2 | a0001 | c0004 | t0017 | g0107 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0332 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02293 | hp1 | a0001 | c0003 | t0003 | g0268 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02451 | hp1 | a0001 | c0003 | t0010 | g0340 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0147 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0229 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02622 | hp1 | a0001 | c0002 | t0008 | g0077 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02622 | hp2 | a0001 | c0003 | t0016 | g0321 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0231 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02647 | hp1 | a0001 | c0003 | t0012 | g0304 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02647 | hp2 | a0001 | c0001 | t0015 | g0224 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02683 | hp2 | a0001 | c0003 | t0021 | g0318 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0316 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0074 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0329 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0079 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0076 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0327 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02896 | hp2 | a0001 | c0003 | t0003 | g0335 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0334 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02922 | hp1 | a0001 | c0001 | t0019 | g0217 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02922 | hp2 | a0001 | c0002 | t0008 | g0065 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0115 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02965 | hp2 | a0001 | c0003 | t0010 | g0337 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02970 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0233 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0070 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0325 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0097 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0066 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03098 | hp2 | a0001 | c0003 | t0005 | g0301 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03139 | hp1 | a0001 | c0003 | t0010 | g0338 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0096 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03225 | hp2 | a0001 | c0003 | t0014 | g0298 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03239 | hp1 | a0001 | c0003 | t0007 | g0309 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0210 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0336 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0071 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0256 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0206 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03516 | hp1 | a0001 | c0003 | t0011 | g0323 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0073 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0223 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0330 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0315 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03831 | hp1 | a0001 | c0003 | t0003 | g0260 | SAS | BEB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | BEB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0324 | SAS | BEB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | BEB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04115 | hp1 | a0001 | c0001 | t0029 | g0162 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04199 | hp2 | a0001 | c0003 | t0024 | g0326 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04204 | hp2 | a0001 | c0003 | t0003 | g0259 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0189 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04228 | hp2 | a0001 | c0003 | t0003 | g0276 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0116 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18747 | hp2 | a0001 | c0003 | t0009 | g0267 | EAS | CHB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18906 | hp1 | a0001 | c0003 | t0005 | g0300 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0240 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18939 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18939 | hp2 | a0001 | c0001 | t0009 | g0138 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18942 | hp1 | a0002 | c0005 | t0001 | g0341 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0295 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18946 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0281 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18959 | hp2 | a0001 | c0003 | t0003 | g0273 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18960 | hp1 | a0001 | c0003 | t0003 | g0293 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18961 | hp2 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0269 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18964 | hp1 | a0001 | c0002 | t0009 | g0086 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18968 | hp1 | a0001 | c0001 | t0028 | g0119 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18968 | hp2 | a0001 | c0003 | t0003 | g0254 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18970 | hp1 | a0001 | c0002 | t0004 | g0099 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18971 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18973 | hp1 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18974 | hp1 | a0001 | c0001 | t0025 | g0140 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0285 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0103 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18979 | hp2 | a0001 | c0003 | t0003 | g0287 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18981 | hp2 | a0001 | c0003 | t0003 | g0271 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18985 | hp1 | a0001 | c0003 | t0003 | g0262 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0020 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18998 | hp1 | a0001 | c0003 | t0003 | g0282 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18999 | hp2 | a0001 | c0003 | t0003 | g0288 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0253 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19002 | hp1 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19003 | hp1 | a0001 | c0002 | t0009 | g0100 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0296 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19030 | hp1 | a0001 | c0003 | t0011 | g0322 | AFR | LWK | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | LWK | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0331 | AFR | LWK | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19043 | hp2 | a0001 | c0002 | t0008 | g0078 | AFR | LWK | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0275 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19057 | hp1 | a0001 | c0002 | t0005 | g0091 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19058 | hp1 | a0001 | c0003 | t0003 | g0255 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19058 | hp2 | a0001 | c0002 | t0022 | g0018 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19062 | hp1 | a0001 | c0002 | t0004 | g0102 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19062 | hp2 | a0001 | c0003 | t0003 | g0286 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0284 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19070 | hp1 | a0001 | c0003 | t0003 | g0272 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19074 | hp1 | a0001 | c0003 | t0003 | g0280 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19081 | hp2 | a0001 | c0001 | t0027 | g0121 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0297 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19085 | hp1 | a0001 | c0002 | t0005 | g0021 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19085 | hp2 | a0001 | c0003 | t0003 | g0277 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19086 | hp2 | a0001 | c0003 | t0003 | g0292 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19090 | hp1 | a0001 | c0003 | t0003 | g0278 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19091 | hp1 | a0001 | c0003 | t0003 | g0291 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0245 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19240 | hp2 | a0001 | c0001 | t0018 | g0230 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0257 | AFR | ASW | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | ASW | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0030 | EUR | TSI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0075 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0241 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02486 | hp1 | a0001 | c0003 | t0003 | g0320 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0333 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02559 | hp1 | a0001 | c0002 | t0008 | g0072 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02559 | hp2 | a0001 | c0001 | t0030 | g0252 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03471 | hp1 | a0001 | c0002 | t0005 | g0069 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03471 | hp2 | a0001 | c0003 | t0010 | g0339 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | USA | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0095 | AFR | USA | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0236 | AFR | USA | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0183 | REF | REF | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0163 | REF | REF | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123585009
|
T | A | 1 | a0002 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.19A>T | p.Thr7Ser | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 45/4125 | 19/765 | 7/254 | chr3 | 123585009 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123584965
|
C | T | 1 | a0001c0004 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.63G>A | p.Gly21Gly | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 89/4125 | 63/765 | 21/254 | chr3 | 123584965 | ||
| chr3:123584974
|
G | C | 3 | a0001c0002a0001c0003a0002c0005 | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(194): Show |
synonymous_variant | LOW | c.54C>G | p.Gly18Gly | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 80/4125 | 54/765 | 18/254 | chr3 | 123584974 | ||
| chr3:123584977
|
A | G | 2 | a0001c0002a0002c0005 | 103 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(100): Show |
synonymous_variant | LOW | c.51T>C | p.Gly17Gly | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 77/4125 | 51/765 | 17/254 | chr3 | 123584977 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123491817
|
C | T | 3 | a0001c0001t0013a0001c0003t0007a0001c0003t0014 | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3071G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 3071 | chr3 | 123491817 | |||||
| chr3:123491852
|
C | A | 1 | a0001c0003t0026 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3036G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 3036 | chr3 | 123491852 | |||||
| chr3:123491968
|
A | T | 4 | a0001c0001t0009a0001c0002t0009a0001c0002t0022others(1): Show | 5 | NA18747.hp2 NA18939.hp2 NA18964.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2920T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2920 | chr3 | 123491968 | |||||
| chr3:123492030
|
C | G | 1 | a0001c0002t0023 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2858G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2858 | chr3 | 123492030 | |||||
| chr3:123492046
|
C | G | 1 | a0001c0001t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2842G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2842 | chr3 | 123492046 | |||||
| chr3:123492111
|
C | T | 1 | a0001c0002t0020 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2777G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2777 | chr3 | 123492111 | |||||
| chr3:123492131
|
T | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*2757A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2757 | chr3 | 123492131 | |||||
| chr3:123492168
|
C | G | 3 | a0001c0001t0013a0001c0003t0007a0001c0003t0014 | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2720G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2720 | chr3 | 123492168 | |||||
| chr3:123492168
|
C | T | 1 | a0001c0001t0029 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2720G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2720 | chr3 | 123492168 | |||||
| chr3:123492178
|
T | C | 1 | a0001c0003t0024 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2710A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2710 | chr3 | 123492178 | |||||
| chr3:123492217
|
G | T | 3 | a0001c0001t0004a0001c0001t0031a0001c0002t0004 | 40 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2671C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2671 | chr3 | 123492217 | |||||
| chr3:123492301
|
CCTTTGAC others(47): Show |
C | 1 | a0001c0001t0028 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2533_*2586delTTTT others(50): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2533 | chr3 | 123492301 | |||||
| chr3:123492448
|
G | A | 3 | a0001c0001t0005a0001c0002t0005a0001c0003t0005 | 26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2440C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2440 | chr3 | 123492448 | |||||
| chr3:123492568
|
C | T | 1 | a0001c0003t0007 | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2320G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2320 | chr3 | 123492568 | |||||
| chr3:123493006
|
C | T | 1 | a0001c0002t0022 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1882G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1882 | chr3 | 123493006 | |||||
| chr3:123493022
|
A | G | 1 | a0001c0001t0027 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1866T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1866 | chr3 | 123493022 | |||||
| chr3:123493032
|
A | G | 1 | a0001c0001t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1856T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1856 | chr3 | 123493032 | |||||
| chr3:123493120
|
T | C | 3 | a0001c0001t0013a0001c0003t0007a0001c0003t0014 | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1768A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1768 | chr3 | 123493120 | |||||
| chr3:123493190
|
T | C | 3 | a0001c0001t0013a0001c0003t0007a0001c0003t0014 | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1698A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1698 | chr3 | 123493190 | |||||
| chr3:123493196
|
T | C | 13 | a0001c0001t0002a0001c0001t0004a0001c0001t0025others(10): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1692A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1692 | chr3 | 123493196 | |||||
| chr3:123493205
|
A | C | 1 | a0001c0001t0018 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1683T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1683 | chr3 | 123493205 | |||||
| chr3:123493225
|
A | G | 1 | a0001c0003t0021 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1663 | chr3 | 123493225 | |||||
| chr3:123493229
|
A | G | 1 | a0001c0003t0021 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1659T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1659 | chr3 | 123493229 | |||||
| chr3:123493304
|
T | C | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*1584A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1584 | chr3 | 123493304 | |||||
| chr3:123493335
|
A | G | 1 | a0001c0002t0020 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1553T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1553 | chr3 | 123493335 | |||||
| chr3:123493342
|
C | T | 1 | a0001c0002t0008 | 7 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1546G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1546 | chr3 | 123493342 | |||||
| chr3:123493351
|
G | A | 1 | a0001c0001t0019 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1537C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1537 | chr3 | 123493351 | |||||
| chr3:123493423
|
A | T | 1 | a0001c0003t0010 | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1465T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1465 | chr3 | 123493423 | |||||
| chr3:123493716
|
A | G | 12 | a0001c0001t0001a0001c0001t0009a0001c0002t0001others(9): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1172T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1172 | chr3 | 123493716 | |||||
| chr3:123493847
|
A | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*1041T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1041 | chr3 | 123493847 | |||||
| chr3:123493848
|
G | A | 1 | a0001c0001t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1040C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1040 | chr3 | 123493848 | |||||
| chr3:123493985
|
C | T | 3 | a0001c0001t0013a0001c0003t0007a0001c0003t0014 | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*903G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 903 | chr3 | 123493985 | |||||
| chr3:123494025
|
C | T | 1 | a0001c0004t0017 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*863G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 863 | chr3 | 123494025 | |||||
| chr3:123494079
|
C | T | 1 | a0001c0003t0012 | 2 | HG01884.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*809G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 809 | chr3 | 123494079 | |||||
| chr3:123494086
|
T | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*802A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 802 | chr3 | 123494086 | |||||
| chr3:123494172
|
T | C | 1 | a0001c0003t0014 | 2 | HG02055.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*716A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 716 | chr3 | 123494172 | |||||
| chr3:123494456
|
C | G | 1 | a0001c0004t0017 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 432 | chr3 | 123494456 | |||||
| chr3:123494478
|
C | T | 2 | a0001c0003t0011a0001c0003t0016 | 3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 410 | chr3 | 123494478 | |||||
| chr3:123494589
|
A | G | 1 | a0001c0003t0016 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 299 | chr3 | 123494589 | |||||
| chr3:123494702
|
T | C | 1 | a0001c0001t0015 | 2 | HG02647.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*186A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 186 | chr3 | 123494702 | |||||
| chr3:123585028
|
G | A | 1 | a0001c0001t0031 | 1 | HG01515.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 1 | chr3 | 123585028 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123495048
|
T | C | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-78A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495048 | ||||||
| chr3:123495122
|
A | G | 1 | a0001c0002t0001g0050 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.683-152T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495122 | ||||||
| chr3:123495181
|
T | C | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.683-211A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495181 | ||||||
| chr3:123495243
|
C | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-273G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495243 | ||||||
| chr3:123495260
|
C | T | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.683-290G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495260 | ||||||
| chr3:123495523
|
C | T | 3 | a0001c0003t0011g0322a0001c0003t0011g0323a0001c0003t0016g0321 | 3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.683-553G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495523 | ||||||
| chr3:123495596
|
TA | T | 81 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(78): Show | 83 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.683-627delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495596 | ||||||
| chr3:123495596
|
TAAAA | T | 221 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(218): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.683-630_683-627del others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495596 | ||||||
| chr3:123495740
|
T | C | 1 | a0001c0001t0004g0208 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.683-770A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495740 | ||||||
| chr3:123495785
|
G | A | 1 | a0001c0003t0003g0296 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.683-815C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495785 | ||||||
| chr3:123495903
|
G | T | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.683-933C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495903 | ||||||
| chr3:123495943
|
G | GTTT | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-974_683-973ins others(3): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495943 | ||||||
| chr3:123496105
|
T | C | 314 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(311): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.683-1135A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496105 | ||||||
| chr3:123496113
|
T | G | 1 | a0001c0001t0004g0205 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.683-1143A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496113 | ||||||
| chr3:123496175
|
C | T | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-1205G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496175 | ||||||
| chr3:123496270
|
G | A | 111 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(108): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.683-1300C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496270 | ||||||
| chr3:123496434
|
A | T | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-1464T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496434 | ||||||
| chr3:123496458
|
C | T | 1 | a0001c0002t0005g0067 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.683-1488G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496458 | ||||||
| chr3:123496462
|
G | A | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-1492C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496462 | ||||||
| chr3:123496600
|
G | A | 108 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(105): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.683-1630C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496600 | ||||||
| chr3:123496656
|
C | G | 4 | a0001c0001t0006g0238a0001c0001t0006g0241a0001c0001t0006g0245others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-1686G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496656 | ||||||
| chr3:123496685
|
A | G | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.683-1715T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496685 | ||||||
| chr3:123496764
|
T | A | 314 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(311): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.683-1794A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496764 | ||||||
| chr3:123496901
|
C | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-1931G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496901 | ||||||
| chr3:123497179
|
C | A | 1 | a0001c0003t0003g0256 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.683-2209G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497179 | ||||||
| chr3:123497261
|
C | T | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-2291G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497261 | ||||||
| chr3:123497346
|
A | T | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.683-2376T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497346 | ||||||
| chr3:123497367
|
C | T | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-2397G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497367 | ||||||
| chr3:123497375
|
G | A | 1 | a0001c0001t0006g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683-2405C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497375 | ||||||
| chr3:123497952
|
G | A | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682+2563C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497952 | ||||||
| chr3:123498242
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.682+2273G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498242 | ||||||
| chr3:123498248
|
T | C | 1 | a0001c0003t0021g0318 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.682+2267A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498248 | ||||||
| chr3:123498358
|
A | T | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.682+2157T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498358 | ||||||
| chr3:123498402
|
A | G | 223 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(220): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.682+2113T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498402 | ||||||
| chr3:123498461
|
G | A | 7 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+2054C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498461 | ||||||
| chr3:123498495
|
C | A | 109 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.682+2020G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498495 | ||||||
| chr3:123498505
|
T | G | 109 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.682+2010A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498505 | ||||||
| chr3:123498625
|
G | A | 1 | a0001c0002t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.682+1890C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498625 | ||||||
| chr3:123498657
|
C | T | 1 | a0001c0002t0001g0022 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.682+1858G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498657 | ||||||
| chr3:123498839
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682+1676G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498839 | ||||||
| chr3:123498860
|
T | C | 1 | a0001c0003t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.682+1655A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498860 | ||||||
| chr3:123498885
|
G | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1630C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498885 | ||||||
| chr3:123498897
|
C | G | 1 | a0001c0001t0002g0005 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.682+1618G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498897 | ||||||
| chr3:123498922
|
A | G | 26 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(23): Show | 26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+1593T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498922 | ||||||
| chr3:123499001
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.682+1514A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499001 | ||||||
| chr3:123499201
|
T | G | 3 | a0001c0001t0002g0220a0001c0001t0013g0115a0001c0001t0013g0116 | 3 | HG02630.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682+1314A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499201 | ||||||
| chr3:123499261
|
T | TA | 46 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(43): Show | 48 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.682+1253dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499261 | ||||||
| chr3:123499298
|
C | T | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+1217G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499298 | ||||||
| chr3:123499366
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.682+1149A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499366 | ||||||
| chr3:123499382
|
G | C | 26 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(23): Show | 26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+1133C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499382 | ||||||
| chr3:123499484
|
C | A | 1 | a0001c0002t0005g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.682+1031G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499484 | ||||||
| chr3:123499578
|
T | C | 1 | a0001c0001t0004g0190 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.682+937A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499578 | ||||||
| chr3:123499607
|
C | G | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+908G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499607 | ||||||
| chr3:123499629
|
G | C | 1 | a0001c0001t0002g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.682+886C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499629 | ||||||
| chr3:123499677
|
TTAAAA | T | 26 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(23): Show | 26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+833_682+837del others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499677 | ||||||
| chr3:123499704
|
T | G | 3 | a0001c0003t0003g0253a0001c0003t0003g0283a0001c0003t0003g0284 | 3 | NA19000.hp2 NA19002.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.682+811A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499704 | ||||||
| chr3:123499801
|
T | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+714A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499801 | ||||||
| chr3:123500131
|
T | A | 1 | a0001c0002t0004g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.682+384A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123500131 | ||||||
| chr3:123500132
|
C | T | 1 | a0001c0002t0004g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.682+383G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123500132 | ||||||
| chr3:123500133
|
T | C | 1 | a0001c0002t0004g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.682+382A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123500133 | ||||||
| chr3:123500290
|
G | A | 223 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(220): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.682+225C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123500290 | ||||||
| chr3:123500910
|
C | T | 1 | a0001c0002t0003g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.504-217G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123500910 | ||||||
| chr3:123501172
|
T | A | 26 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(23): Show | 26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.504-479A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501172 | ||||||
| chr3:123501178
|
TC | T | 26 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(23): Show | 26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.504-486delG | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501178 | ||||||
| chr3:123501218
|
A | G | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.504-525T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501218 | ||||||
| chr3:123501391
|
C | T | 1 | a0001c0003t0003g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.504-698G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501391 | ||||||
| chr3:123501417
|
T | C | 107 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(104): Show | 109 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.504-724A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501417 | ||||||
| chr3:123501443
|
T | G | 1 | a0001c0001t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.504-750A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501443 | ||||||
| chr3:123501587
|
GA | G | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.504-895delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501587 | ||||||
| chr3:123501589
|
A | G | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.504-896T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501589 | ||||||
| chr3:123501714
|
G | A | 78 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(75): Show | 80 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.503+846C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501714 | ||||||
| chr3:123501741
|
T | C | 1 | a0001c0001t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.503+819A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501741 | ||||||
| chr3:123502229
|
T | C | 108 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(105): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.503+331A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123502229 | ||||||
| chr3:123502289
|
A | ATTTTTT | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.503+265_503+270dup others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123502289 | ||||||
| chr3:123502342
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.503+218A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123502342 | ||||||
| chr3:123502781
|
G | A | 2 | a0001c0001t0015g0223a0001c0001t0015g0224 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.382-100C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123502781 | ||||||
| chr3:123502936
|
C | T | 3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382-255G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123502936 | ||||||
| chr3:123502955
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.382-274C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123502955 | ||||||
| chr3:123503188
|
C | T | 17 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.382-507G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503188 | ||||||
| chr3:123503250
|
G | A | 1 | a0001c0003t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.382-569C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503250 | ||||||
| chr3:123503262
|
C | CA | 45 | a0001c0001t0002g0131a0001c0001t0002g0137a0001c0001t0002g0213others(42): Show | 45 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.382-582dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503262 | ||||||
| chr3:123503292
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.382-611A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503292 | ||||||
| chr3:123503447
|
C | G | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-766G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503447 | ||||||
| chr3:123503458
|
T | C | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-777A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503458 | ||||||
| chr3:123503521
|
A | G | 16 | a0001c0001t0004g0175a0001c0001t0004g0179a0001c0001t0004g0180others(13): Show | 16 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.382-840T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503521 | ||||||
| chr3:123503708
|
C | CA | 18 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0002g0133others(15): Show | 18 | HG00597.hp1 HG01884.hp2 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.382-1028dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | ||||||
| chr3:123503708
|
C | CAA | 16 | a0001c0001t0002g0221a0001c0001t0002g0251a0001c0002t0001g0026others(13): Show | 16 | HG02145.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.382-1029_382-1028d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | ||||||
| chr3:123503708
|
C | CAAA | 94 | a0001c0001t0002g0220a0001c0001t0005g0113a0001c0001t0005g0114others(91): Show | 95 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-1030_382-1028d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | ||||||
| chr3:123503708
|
C | CAAAA | 14 | a0001c0002t0001g0015a0001c0002t0001g0082a0001c0002t0020g0056others(11): Show | 14 | HG01993.hp2 HG02080.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.382-1031_382-1028d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | ||||||
| chr3:123503708
|
C | CAAAAA | 40 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(37): Show | 42 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(39): Show |
intron_variant | MODIFIER | c.382-1032_382-1028d others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | ||||||
| chr3:123503708
|
CA | C | 10 | a0001c0001t0001g0152a0001c0001t0002g0126a0001c0001t0002g0142others(7): Show | 10 | HG00558.hp1 HG01884.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-1028delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | ||||||
| chr3:123503716
|
A | C | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-1035T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503716 | ||||||
| chr3:123503761
|
C | T | 1 | a0001c0002t0005g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.382-1080G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503761 | ||||||
| chr3:123503765
|
C | T | 1 | a0001c0003t0003g0290 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.382-1084G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503765 | ||||||
| chr3:123503773
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.382-1092G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503773 | ||||||
| chr3:123504192
|
A | G | 3 | a0001c0003t0011g0322a0001c0003t0011g0323a0001c0003t0016g0321 | 3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.382-1511T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504192 | ||||||
| chr3:123504293
|
G | A | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-1612C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504293 | ||||||
| chr3:123504322
|
A | T | 3 | a0001c0003t0011g0322a0001c0003t0011g0323a0001c0003t0016g0321 | 3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.382-1641T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504322 | ||||||
| chr3:123504453
|
T | G | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-1772A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504453 | ||||||
| chr3:123504503
|
G | A | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.382-1822C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504503 | ||||||
| chr3:123504530
|
T | TA | 14 | a0001c0001t0002g0128a0001c0001t0006g0239a0001c0003t0003g0256others(11): Show | 14 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.382-1850dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504530 | ||||||
| chr3:123504560
|
C | T | 1 | a0001c0003t0003g0275 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.382-1879G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504560 | ||||||
| chr3:123504774
|
C | G | 316 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(313): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.382-2093G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504774 | ||||||
| chr3:123504832
|
A | G | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-2151T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504832 | ||||||
| chr3:123504887
|
A | AAATGT | 340 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(337): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.382-2207_382-2206i others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504887 | ||||||
| chr3:123505041
|
G | A | 18 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(15): Show | 18 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.382-2360C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505041 | ||||||
| chr3:123505223
|
G | A | 5 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-2542C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505223 | ||||||
| chr3:123505315
|
A | G | 1 | a0001c0002t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.382-2634T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505315 | ||||||
| chr3:123505516
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.382-2835C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505516 | ||||||
| chr3:123505601
|
A | G | 1 | a0001c0001t0004g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.382-2920T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505601 | ||||||
| chr3:123505700
|
T | C | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-3019A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505700 | ||||||
| chr3:123505904
|
T | C | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-3223A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505904 | ||||||
| chr3:123506007
|
C | T | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-3326G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506007 | ||||||
| chr3:123506041
|
G | A | 26 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(23): Show | 26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-3360C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506041 | ||||||
| chr3:123506058
|
A | G | 115 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(112): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.382-3377T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506058 | ||||||
| chr3:123506377
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-3696G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506377 | ||||||
| chr3:123506447
|
C | G | 27 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(24): Show | 27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.382-3766G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506447 | ||||||
| chr3:123506617
|
T | C | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-3936A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506617 | ||||||
| chr3:123506776
|
GT | G | 3 | a0001c0003t0003g0256a0001c0003t0003g0257a0001c0003t0003g0258 | 3 | HG01109.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-4096delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506776 | ||||||
| chr3:123506924
|
A | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-4243T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506924 | ||||||
| chr3:123506965
|
A | G | 1 | a0001c0002t0020g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.382-4284T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506965 | ||||||
| chr3:123507006
|
C | T | 108 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(105): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.382-4325G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507006 | ||||||
| chr3:123507069
|
C | A | 1 | a0001c0002t0001g0053 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.382-4388G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507069 | ||||||
| chr3:123507085
|
C | T | 1 | a0001c0001t0009g0138 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.382-4404G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507085 | ||||||
| chr3:123507169
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-4488A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507169 | ||||||
| chr3:123507388
|
G | GAT | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-4709_382-4708d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507388 | ||||||
| chr3:123507507
|
A | T | 1 | a0001c0001t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.382-4826T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507507 | ||||||
| chr3:123507509
|
C | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-4828G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507509 | ||||||
| chr3:123507533
|
C | T | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-4852G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507533 | ||||||
| chr3:123507705
|
A | G | 1 | a0001c0001t0031g0342 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.382-5024T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507705 | ||||||
| chr3:123507730
|
T | A | 2 | a0001c0003t0003g0329a0001c0003t0003g0336 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.382-5049A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507730 | ||||||
| chr3:123507746
|
A | T | 313 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(310): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.382-5065T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507746 | ||||||
| chr3:123507892
|
G | A | 36 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(33): Show | 36 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.382-5211C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507892 | ||||||
| chr3:123507993
|
T | C | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-5312A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507993 | ||||||
| chr3:123508006
|
G | GA | 5 | a0001c0002t0001g0053a0001c0003t0010g0337a0001c0003t0010g0338others(2): Show | 5 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5326dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508006 | ||||||
| chr3:123508006
|
GA | G | 20 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(17): Show | 21 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.382-5326delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508006 | ||||||
| chr3:123508149
|
T | C | 1 | a0001c0001t0013g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382-5468A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508149 | ||||||
| chr3:123508198
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-5517A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508198 | ||||||
| chr3:123508221
|
G | C | 2 | a0001c0001t0015g0223a0001c0001t0015g0224 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.382-5540C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508221 | ||||||
| chr3:123508357
|
G | A | 1 | a0001c0003t0021g0318 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-5676C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508357 | ||||||
| chr3:123508641
|
A | C | 5 | a0001c0001t0005g0139a0001c0002t0005g0020a0001c0002t0005g0021others(2): Show | 5 | HG00673.hp2 NA18994.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5960T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508641 | ||||||
| chr3:123508827
|
T | G | 1 | a0001c0001t0004g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.382-6146A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508827 | ||||||
| chr3:123508848
|
C | A | 1 | a0001c0003t0005g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.382-6167G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508848 | ||||||
| chr3:123508862
|
G | A | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-6181C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508862 | ||||||
| chr3:123508867
|
G | T | 1 | a0001c0002t0005g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382-6186C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508867 | ||||||
| chr3:123508997
|
A | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-6316T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508997 | ||||||
| chr3:123509020
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.382-6339A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509020 | ||||||
| chr3:123509034
|
C | T | 3 | a0001c0001t0006g0233a0001c0001t0006g0237a0001c0001t0006g0242 | 3 | HG02897.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.382-6353G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509034 | ||||||
| chr3:123509094
|
C | T | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.382-6413G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509094 | ||||||
| chr3:123509284
|
C | T | 4 | a0001c0001t0004g0179a0001c0001t0004g0180a0001c0001t0004g0183others(1): Show | 4 | HG00642.hp1 HG01261.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-6603G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509284 | ||||||
| chr3:123509288
|
A | G | 25 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.382-6607T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509288 | ||||||
| chr3:123509428
|
G | A | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-6747C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509428 | ||||||
| chr3:123509500
|
TTC | T | 108 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(105): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.382-6821_382-6820d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509500 | ||||||
| chr3:123509502
|
CT | C | 208 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(205): Show | 212 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.382-6822delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509502 | ||||||
| chr3:123509502
|
CTT | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-6823_382-6822d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509502 | ||||||
| chr3:123509532
|
T | C | 8 | a0001c0002t0001g0015a0001c0002t0001g0081a0001c0002t0001g0082others(5): Show | 8 | NA18962.hp1 NA18972.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-6851A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509532 | ||||||
| chr3:123509599
|
C | T | 269 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(266): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.382-6918G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509599 | ||||||
| chr3:123509623
|
T | C | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-6942A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509623 | ||||||
| chr3:123509641
|
G | A | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-6960C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509641 | ||||||
| chr3:123509652
|
C | A | 8 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0330others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-6971G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509652 | ||||||
| chr3:123509662
|
C | A | 1 | a0001c0001t0006g0231 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382-6981G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509662 | ||||||
| chr3:123509701
|
G | A | 1 | a0001c0003t0005g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.382-7020C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509701 | ||||||
| chr3:123509706
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-7025T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509706 | ||||||
| chr3:123509745
|
C | T | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-7064G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509745 | ||||||
| chr3:123509787
|
G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-7106C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509787 | ||||||
| chr3:123509863
|
G | A | 3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382-7182C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509863 | ||||||
| chr3:123509864
|
G | GGGAGAAG others(9): Show |
2 | a0001c0003t0003g0329a0001c0003t0003g0336 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.382-7199_382-7184d others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509864 | ||||||
| chr3:123509940
|
G | C | 2 | a0001c0001t0004g0109a0001c0001t0004g0110 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.382-7259C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509940 | ||||||
| chr3:123510333
|
C | T | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-7652G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510333 | ||||||
| chr3:123510340
|
C | T | 2 | a0001c0003t0003g0334a0001c0003t0003g0335 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.382-7659G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510340 | ||||||
| chr3:123510341
|
G | T | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-7660C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510341 | ||||||
| chr3:123510395
|
C | G | 3 | a0001c0003t0003g0269a0001c0003t0003g0270a0001c0003t0003g0272 | 3 | HG02129.hp2 NA18962.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.382-7714G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510395 | ||||||
| chr3:123510456
|
C | T | 6 | a0001c0002t0001g0014a0001c0002t0001g0080a0001c0002t0001g0085others(3): Show | 6 | NA18959.hp1 NA18964.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-7775G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510456 | ||||||
| chr3:123510465
|
C | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-7784G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510465 | ||||||
| chr3:123510473
|
C | G | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-7792G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510473 | ||||||
| chr3:123510535
|
A | C | 1 | a0001c0001t0002g0155 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.382-7854T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510535 | ||||||
| chr3:123510541
|
G | A | 1 | a0001c0002t0020g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.382-7860C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510541 | ||||||
| chr3:123510631
|
T | C | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-7950A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510631 | ||||||
| chr3:123510716
|
G | T | 97 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(94): Show | 99 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.382-8035C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510716 | ||||||
| chr3:123510818
|
T | A | 1 | a0001c0002t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.382-8137A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510818 | ||||||
| chr3:123510932
|
GT | G | 258 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(255): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.382-8252delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510932 | ||||||
| chr3:123510932
|
GTT | G | 58 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251others(55): Show | 60 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(57): Show |
intron_variant | MODIFIER | c.382-8253_382-8252d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510932 | ||||||
| chr3:123510932
|
GTTT | G | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-8254_382-8252d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510932 | ||||||
| chr3:123510933
|
T | G | 3 | a0001c0002t0001g0048a0001c0002t0001g0089a0001c0002t0001g0090 | 3 | HG03490.hp2 NA18972.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.382-8252A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510933 | ||||||
| chr3:123510934
|
T | G | 109 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(106): Show | 111 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.382-8253A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510934 | ||||||
| chr3:123510935
|
T | G | 1 | a0001c0003t0003g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382-8254A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510935 | ||||||
| chr3:123510944
|
T | G | 5 | a0001c0001t0002g0129a0001c0001t0006g0218a0001c0001t0006g0244others(2): Show | 5 | HG01358.hp2 HG02257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-8263A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510944 | ||||||
| chr3:123510945
|
G | T | 5 | a0001c0001t0002g0129a0001c0001t0006g0218a0001c0001t0006g0244others(2): Show | 5 | HG01358.hp2 HG02257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-8264C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510945 | ||||||
| chr3:123510955
|
G | T | 1 | a0001c0001t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.382-8274C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510955 | ||||||
| chr3:123510955
|
GT | G | 81 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(78): Show | 83 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.382-8275delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510955 | ||||||
| chr3:123510955
|
GTT | G | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-8276_382-8275d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510955 | ||||||
| chr3:123510956
|
T | G | 1 | a0001c0001t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.382-8275A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510956 | ||||||
| chr3:123510963
|
T | G | 7 | a0001c0002t0008g0013a0001c0002t0008g0065a0001c0002t0008g0070others(4): Show | 7 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-8282A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510963 | ||||||
| chr3:123511007
|
A | G | 93 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(90): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-8326T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511007 | ||||||
| chr3:123511047
|
G | C | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-8366C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511047 | ||||||
| chr3:123511159
|
C | T | 4 | a0001c0001t0005g0139a0001c0002t0005g0020a0001c0002t0005g0021others(1): Show | 4 | NA18994.hp2 NA19057.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-8478G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511159 | ||||||
| chr3:123511278
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-8597A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511278 | ||||||
| chr3:123511496
|
T | C | 7 | a0001c0002t0008g0013a0001c0002t0008g0065a0001c0002t0008g0070others(4): Show | 7 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-8815A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511496 | ||||||
| chr3:123511618
|
G | A | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-8937C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511618 | ||||||
| chr3:123511726
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.382-9045C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511726 | ||||||
| chr3:123511808
|
C | G | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-9127G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511808 | ||||||
| chr3:123511925
|
G | A | 1 | a0001c0001t0004g0183 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.382-9244C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511925 | ||||||
| chr3:123511930
|
C | T | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.382-9249G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511930 | ||||||
| chr3:123511954
|
C | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-9273G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511954 | ||||||
| chr3:123512221
|
C | T | 5 | a0001c0002t0005g0094a0001c0002t0005g0095a0001c0002t0005g0096others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-9540G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512221 | ||||||
| chr3:123512288
|
G | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.382-9607C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512288 | ||||||
| chr3:123512305
|
A | C | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-9624T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512305 | ||||||
| chr3:123512413
|
C | T | 1 | a0001c0001t0004g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.382-9732G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512413 | ||||||
| chr3:123512487
|
A | T | 97 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(94): Show | 99 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.382-9806T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512487 | ||||||
| chr3:123512883
|
G | T | 4 | a0001c0001t0005g0139a0001c0002t0005g0020a0001c0002t0005g0021others(1): Show | 4 | NA18994.hp2 NA19057.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-10202C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512883 | ||||||
| chr3:123513058
|
A | G | 108 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(105): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.382-10377T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513058 | ||||||
| chr3:123513287
|
T | C | 93 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(90): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-10606A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513287 | ||||||
| chr3:123513354
|
C | G | 1 | a0001c0001t0006g0245 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.382-10673G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513354 | ||||||
| chr3:123513404
|
T | C | 93 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(90): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-10723A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513404 | ||||||
| chr3:123513470
|
C | T | 1 | a0001c0003t0003g0294 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.382-10789G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513470 | ||||||
| chr3:123513789
|
C | T | 1 | a0001c0001t0004g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.382-11108G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513789 | ||||||
| chr3:123513846
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-11165A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513846 | ||||||
| chr3:123513860
|
G | C | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-11179C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513860 | ||||||
| chr3:123514052
|
A | T | 52 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(49): Show | 54 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(51): Show |
intron_variant | MODIFIER | c.382-11371T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514052 | ||||||
| chr3:123514100
|
C | T | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-11419G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514100 | ||||||
| chr3:123514189
|
C | T | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-11508G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514189 | ||||||
| chr3:123514350
|
G | A | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.382-11669C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514350 | ||||||
| chr3:123514360
|
T | C | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-11679A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514360 | ||||||
| chr3:123514361
|
G | A | 1 | a0001c0001t0006g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-11680C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514361 | ||||||
| chr3:123514419
|
AATTGTTT others(3): Show |
A | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-11748_382-1173 others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514419 | ||||||
| chr3:123514429
|
T | TA | 221 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(218): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.382-11749dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514429 | ||||||
| chr3:123514430
|
A | C | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-11749T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514430 | ||||||
| chr3:123514480
|
A | C | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-11799T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514480 | ||||||
| chr3:123514608
|
T | C | 93 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(90): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-11927A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514608 | ||||||
| chr3:123514926
|
G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-12245C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514926 | ||||||
| chr3:123515101
|
T | C | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.382-12420A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515101 | ||||||
| chr3:123515113
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.382-12432G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515113 | ||||||
| chr3:123515138
|
G | A | 46 | a0001c0001t0002g0003a0001c0001t0002g0117a0001c0001t0002g0118others(43): Show | 47 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.382-12457C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515138 | ||||||
| chr3:123515202
|
A | C | 2 | a0001c0003t0010g0337a0001c0003t0010g0338 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.382-12521T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515202 | ||||||
| chr3:123515267
|
T | C | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.382-12586A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515267 | ||||||
| chr3:123515274
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.382-12593A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515274 | ||||||
| chr3:123515290
|
C | G | 2 | a0001c0002t0001g0014a0001c0002t0001g0080 | 2 | NA18959.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.382-12609G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515290 | ||||||
| chr3:123515623
|
C | A | 1 | a0001c0002t0001g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.381+12763G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515623 | ||||||
| chr3:123515625
|
T | G | 2 | a0001c0001t0006g0226a0001c0001t0006g0232 | 2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.381+12761A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515625 | ||||||
| chr3:123515715
|
T | C | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.381+12671A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515715 | ||||||
| chr3:123515724
|
A | T | 1 | a0001c0003t0003g0264 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.381+12662T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515724 | ||||||
| chr3:123515744
|
T | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381+12642A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515744 | ||||||
| chr3:123515757
|
G | T | 111 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(108): Show | 113 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.381+12629C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515757 | ||||||
| chr3:123515900
|
G | A | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+12486C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515900 | ||||||
| chr3:123515917
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.381+12469G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515917 | ||||||
| chr3:123515947
|
A | G | 1 | a0001c0002t0005g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.381+12439T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515947 | ||||||
| chr3:123515949
|
G | A | 1 | a0001c0001t0002g0125 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.381+12437C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515949 | ||||||
| chr3:123515989
|
A | G | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+12397T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515989 | ||||||
| chr3:123516135
|
G | C | 1 | a0001c0003t0003g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.381+12251C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516135 | ||||||
| chr3:123516164
|
T | C | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+12222A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516164 | ||||||
| chr3:123516213
|
G | C | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+12173C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516213 | ||||||
| chr3:123516233
|
A | AT | 13 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0225others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+12152dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516233 | ||||||
| chr3:123516233
|
A | ATTT | 8 | a0001c0001t0013g0116a0001c0003t0007g0305a0001c0003t0007g0306others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+12150_381+1215 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516233 | ||||||
| chr3:123516233
|
AT | A | 57 | a0001c0001t0002g0146a0001c0001t0002g0170a0001c0001t0003g0112others(54): Show | 59 | HG00544.hp2 HG00642.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.381+12152delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516233 | ||||||
| chr3:123516233
|
ATT | A | 213 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(210): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.381+12151_381+1215 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516233 | ||||||
| chr3:123516380
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.381+12006C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516380 | ||||||
| chr3:123516383
|
C | T | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+12003G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516383 | ||||||
| chr3:123516542
|
A | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+11844T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516542 | ||||||
| chr3:123516555
|
A | C | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+11831T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516555 | ||||||
| chr3:123516625
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.381+11761C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516625 | ||||||
| chr3:123516782
|
C | G | 1 | a0001c0002t0001g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.381+11604G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516782 | ||||||
| chr3:123516858
|
T | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+11528A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516858 | ||||||
| chr3:123516863
|
G | A | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+11523C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516863 | ||||||
| chr3:123517053
|
T | C | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+11333A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517053 | ||||||
| chr3:123517276
|
T | C | 1 | a0001c0001t0019g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.381+11110A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517276 | ||||||
| chr3:123517359
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+11027G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517359 | ||||||
| chr3:123517371
|
G | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+11015C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517371 | ||||||
| chr3:123517498
|
T | C | 1 | a0001c0003t0024g0326 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+10888A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517498 | ||||||
| chr3:123517546
|
A | T | 1 | a0001c0001t0004g0203 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.381+10840T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517546 | ||||||
| chr3:123517899
|
TAAAAATA others(308): Show |
T | 314 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(311): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.381+10172_381+1048 others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517899 | ||||||
| chr3:123518191
|
C | CAA | 9 | a0001c0001t0006g0219a0001c0001t0006g0225a0001c0001t0006g0226others(6): Show | 9 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+10193_381+1019 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518191 | ||||||
| chr3:123518338
|
C | G | 42 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(39): Show | 42 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.381+10048G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518338 | ||||||
| chr3:123518368
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+10018A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518368 | ||||||
| chr3:123518433
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+9953G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518433 | ||||||
| chr3:123518521
|
AGTTATTT others(6): Show |
A | 4 | a0001c0003t0003g0260a0001c0003t0003g0263a0001c0003t0003g0271others(1): Show | 4 | HG02080.hp2 HG02083.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+9852_381+9864d others(15): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518521 | ||||||
| chr3:123518551
|
A | T | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+9835T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518551 | ||||||
| chr3:123518654
|
A | T | 1 | a0001c0002t0005g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.381+9732T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518654 | ||||||
| chr3:123518670
|
A | G | 111 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(108): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.381+9716T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518670 | ||||||
| chr3:123518905
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.381+9481C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518905 | ||||||
| chr3:123518945
|
C | T | 1 | a0001c0003t0003g0294 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.381+9441G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518945 | ||||||
| chr3:123518952
|
G | A | 1 | a0001c0002t0002g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.381+9434C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518952 | ||||||
| chr3:123518993
|
A | G | 1 | a0001c0002t0003g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.381+9393T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518993 | ||||||
| chr3:123518995
|
T | TA | 18 | a0001c0001t0002g0145a0001c0001t0002g0155a0001c0001t0002g0160others(15): Show | 18 | HG00140.hp1 HG00735.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.381+9390dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518995 | ||||||
| chr3:123518995
|
TA | T | 145 | a0001c0001t0002g0133a0001c0001t0002g0144a0001c0001t0002g0221others(142): Show | 148 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.381+9390delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518995 | ||||||
| chr3:123519086
|
T | C | 2 | a0001c0001t0005g0113a0001c0001t0005g0114 | 2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.381+9300A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519086 | ||||||
| chr3:123519209
|
T | C | 1 | a0001c0003t0001g0317 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.381+9177A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519209 | ||||||
| chr3:123519267
|
C | T | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.381+9119G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519267 | ||||||
| chr3:123519664
|
G | A | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+8722C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519664 | ||||||
| chr3:123519805
|
G | A | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+8581C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519805 | ||||||
| chr3:123519890
|
T | C | 1 | a0001c0001t0004g0206 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.381+8496A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519890 | ||||||
| chr3:123519902
|
A | G | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.381+8484T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519902 | ||||||
| chr3:123519935
|
A | T | 2 | a0001c0003t0003g0256a0001c0003t0003g0258 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.381+8451T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519935 | ||||||
| chr3:123520012
|
G | T | 1 | a0001c0003t0009g0267 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.381+8374C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520012 | ||||||
| chr3:123520096
|
C | T | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+8290G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520096 | ||||||
| chr3:123520099
|
G | A | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.381+8287C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520099 | ||||||
| chr3:123520343
|
C | T | 1 | a0001c0002t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.381+8043G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520343 | ||||||
| chr3:123520403
|
T | G | 1 | a0001c0001t0002g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.381+7983A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520403 | ||||||
| chr3:123520518
|
C | A | 1 | a0001c0002t0001g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.381+7868G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520518 | ||||||
| chr3:123520571
|
A | G | 3 | a0001c0002t0008g0072a0001c0002t0008g0077a0001c0002t0008g0078 | 3 | HG02559.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.381+7815T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520571 | ||||||
| chr3:123521106
|
T | C | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.381+7280A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521106 | ||||||
| chr3:123521152
|
A | C | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+7234T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521152 | ||||||
| chr3:123521256
|
C | T | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+7130G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521256 | ||||||
| chr3:123521283
|
T | C | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+7103A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521283 | ||||||
| chr3:123521416
|
C | G | 27 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(24): Show | 27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+6970G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521416 | ||||||
| chr3:123521449
|
C | T | 1 | a0001c0002t0020g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.381+6937G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521449 | ||||||
| chr3:123521568
|
A | G | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.381+6818T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521568 | ||||||
| chr3:123521600
|
C | CA | 13 | a0001c0001t0004g0110a0001c0001t0013g0115a0001c0001t0013g0116others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+6785dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521600 | ||||||
| chr3:123521600
|
CA | C | 34 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(31): Show | 34 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.381+6785delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521600 | ||||||
| chr3:123521634
|
T | G | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+6752A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521634 | ||||||
| chr3:123521698
|
G | C | 1 | a0001c0003t0003g0258 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.381+6688C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521698 | ||||||
| chr3:123521749
|
A | G | 4 | a0001c0002t0004g0002a0001c0002t0004g0099a0001c0002t0004g0102others(1): Show | 5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+6637T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521749 | ||||||
| chr3:123521874
|
T | C | 1 | a0001c0003t0003g0255 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.381+6512A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521874 | ||||||
| chr3:123521906
|
CA | C | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+6479delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521906 | ||||||
| chr3:123522332
|
C | CA | 132 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(129): Show | 136 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.381+6053dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522332 | ||||||
| chr3:123522332
|
C | CAA | 52 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(49): Show | 54 | HG00544.hp2 HG00738.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.381+6052_381+6053d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522332 | ||||||
| chr3:123522337
|
A | AG | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+6048_381+6049i others(3): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522337 | ||||||
| chr3:123522348
|
A | G | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+6038T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522348 | ||||||
| chr3:123522349
|
AG | A | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+6036delC | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522349 | ||||||
| chr3:123522433
|
A | T | 112 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(109): Show | 116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.381+5953T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522433 | ||||||
| chr3:123522455
|
G | C | 2 | a0001c0003t0005g0301a0001c0003t0005g0302 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.381+5931C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522455 | ||||||
| chr3:123522581
|
A | G | 328 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(325): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.381+5805T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522581 | ||||||
| chr3:123522657
|
G | A | 1 | a0001c0001t0006g0244 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.381+5729C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522657 | ||||||
| chr3:123522662
|
C | CT | 148 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0248others(145): Show | 152 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.381+5723dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522662 | ||||||
| chr3:123522662
|
C | CTT | 94 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.381+5722_381+5723d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522662 | ||||||
| chr3:123522741
|
A | T | 3 | a0001c0003t0003g0256a0001c0003t0003g0257a0001c0003t0003g0258 | 3 | HG01109.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.381+5645T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522741 | ||||||
| chr3:123522875
|
T | C | 27 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(24): Show | 27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+5511A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522875 | ||||||
| chr3:123523161
|
A | G | 25 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.381+5225T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523161 | ||||||
| chr3:123523243
|
A | C | 5 | a0001c0002t0005g0094a0001c0002t0005g0095a0001c0002t0005g0096others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+5143T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523243 | ||||||
| chr3:123523253
|
C | T | 3 | a0001c0001t0001g0150a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG00423.hp2 HG00738.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.381+5133G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523253 | ||||||
| chr3:123523254
|
G | A | 5 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+5132C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523254 | ||||||
| chr3:123523262
|
G | C | 6 | a0001c0002t0001g0014a0001c0002t0001g0080a0001c0002t0001g0085others(3): Show | 6 | NA18959.hp1 NA18964.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+5124C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523262 | ||||||
| chr3:123523373
|
G | A | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+5013C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523373 | ||||||
| chr3:123523427
|
T | C | 10 | a0001c0001t0006g0219a0001c0001t0006g0225a0001c0001t0006g0226others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+4959A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523427 | ||||||
| chr3:123523698
|
G | A | 2 | a0001c0003t0003g0332a0001c0003t0003g0333 | 2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.381+4688C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523698 | ||||||
| chr3:123523777
|
C | T | 1 | a0001c0003t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.381+4609G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523777 | ||||||
| chr3:123524052
|
A | C | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.381+4334T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524052 | ||||||
| chr3:123524312
|
G | A | 1 | a0001c0001t0006g0250 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.381+4074C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524312 | ||||||
| chr3:123524376
|
G | C | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+4010C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524376 | ||||||
| chr3:123524535
|
C | T | 1 | a0001c0001t0018g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.381+3851G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524535 | ||||||
| chr3:123524579
|
C | T | 109 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.381+3807G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524579 | ||||||
| chr3:123524606
|
C | T | 1 | a0001c0003t0005g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+3780G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524606 | ||||||
| chr3:123524797
|
T | C | 2 | a0001c0002t0005g0074a0001c0002t0005g0076 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.381+3589A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524797 | ||||||
| chr3:123524827
|
T | C | 4 | a0001c0002t0004g0002a0001c0002t0004g0099a0001c0002t0004g0102others(1): Show | 5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+3559A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524827 | ||||||
| chr3:123524968
|
G | A | 33 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(30): Show | 33 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.381+3418C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524968 | ||||||
| chr3:123524980
|
C | T | 221 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(218): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.381+3406G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524980 | ||||||
| chr3:123525190
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.381+3196T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525190 | ||||||
| chr3:123525269
|
A | T | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.381+3117T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525269 | ||||||
| chr3:123525404
|
C | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.381+2982G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525404 | ||||||
| chr3:123525481
|
A | C | 1 | a0001c0002t0005g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.381+2905T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525481 | ||||||
| chr3:123525644
|
A | G | 1 | a0001c0001t0004g0188 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.381+2742T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525644 | ||||||
| chr3:123525722
|
A | G | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381+2664T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525722 | ||||||
| chr3:123525749
|
T | C | 1 | a0001c0003t0010g0339 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.381+2637A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525749 | ||||||
| chr3:123526022
|
C | T | 25 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.381+2364G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526022 | ||||||
| chr3:123526041
|
GAGCAAGC others(47): Show |
G | 3 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0001g0325 | 3 | HG02965.hp1 HG03017.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+2291_381+2344d others(56): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526041 | ||||||
| chr3:123526262
|
A | G | 27 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(24): Show | 27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+2124T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526262 | ||||||
| chr3:123526264
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0151 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.381+2122C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526264 | ||||||
| chr3:123526305
|
G | A | 113 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(110): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.381+2081C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526305 | ||||||
| chr3:123526527
|
CTTTTCCT others(10): Show |
C | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+1842_381+1858d others(19): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526527 | ||||||
| chr3:123526533
|
CTT | C | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+1851_381+1852d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526533 | ||||||
| chr3:123526627
|
G | T | 220 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(217): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.381+1759C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526627 | ||||||
| chr3:123526628
|
T | G | 220 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(217): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.381+1758A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526628 | ||||||
| chr3:123527155
|
C | T | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.381+1231G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527155 | ||||||
| chr3:123527230
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.381+1156A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527230 | ||||||
| chr3:123527250
|
G | A | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+1136C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527250 | ||||||
| chr3:123527278
|
C | T | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+1108G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527278 | ||||||
| chr3:123527592
|
G | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+794C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527592 | ||||||
| chr3:123527639
|
G | C | 1 | a0001c0003t0003g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+747C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527639 | ||||||
| chr3:123527663
|
T | C | 1 | a0001c0001t0019g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.381+723A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527663 | ||||||
| chr3:123527731
|
G | T | 71 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(68): Show | 72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.381+655C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527731 | ||||||
| chr3:123527790
|
T | C | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.381+596A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527790 | ||||||
| chr3:123527831
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.381+555C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527831 | ||||||
| chr3:123527874
|
C | T | 73 | a0001c0001t0009g0138a0001c0001t0013g0115a0001c0001t0013g0116others(70): Show | 74 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.381+512G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527874 | ||||||
| chr3:123527931
|
C | T | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381+455G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527931 | ||||||
| chr3:123528304
|
T | C | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.381+82A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123528304 | ||||||
| chr3:123528367
|
G | A | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+19C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123528367 | ||||||
| chr3:123528374
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0145 | 3 | NA18994.hp1 NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.381+12T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123528374 | ||||||
| chr3:123528522
|
C | T | 6 | a0001c0002t0001g0014a0001c0002t0001g0080a0001c0002t0001g0085others(3): Show | 6 | NA18959.hp1 NA18964.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-48G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123528522 | ||||||
| chr3:123528607
|
T | C | 93 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(90): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.293-133A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123528607 | ||||||
| chr3:123528630
|
T | C | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-156A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123528630 | ||||||
| chr3:123528767
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-293A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123528767 | ||||||
| chr3:123529006
|
CT | C | 275 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(272): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.293-533delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529006 | ||||||
| chr3:123529006
|
CTT | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-534_293-533del others(2): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529006 | ||||||
| chr3:123529008
|
T | C | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-534A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529008 | ||||||
| chr3:123529241
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-767G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529241 | ||||||
| chr3:123529329
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.293-855A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529329 | ||||||
| chr3:123529596
|
C | T | 71 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(68): Show | 72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.293-1122G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529596 | ||||||
| chr3:123529800
|
G | A | 2 | a0001c0001t0009g0138a0001c0002t0009g0100 | 2 | NA18939.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.293-1326C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529800 | ||||||
| chr3:123529817
|
G | A | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-1343C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529817 | ||||||
| chr3:123529893
|
GA | G | 5 | a0001c0002t0005g0094a0001c0002t0005g0095a0001c0002t0005g0096others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-1420delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529893 | ||||||
| chr3:123529924
|
A | T | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-1450T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529924 | ||||||
| chr3:123530046
|
T | G | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1572A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530046 | ||||||
| chr3:123530054
|
C | A | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1580G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530054 | ||||||
| chr3:123530056
|
A | C | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1582T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530056 | ||||||
| chr3:123530058
|
T | C | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1584A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530058 | ||||||
| chr3:123530061
|
G | A | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1587C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530061 | ||||||
| chr3:123530064
|
A | T | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1590T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530064 | ||||||
| chr3:123530081
|
T | A | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1607A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530081 | ||||||
| chr3:123530082
|
A | G | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1608T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530082 | ||||||
| chr3:123530083
|
A | ACATTAGT others(30): Show |
1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1610_293-1609i others(39): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530083 | ||||||
| chr3:123530100
|
T | C | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1626A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530100 | ||||||
| chr3:123530111
|
G | A | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1637C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530111 | ||||||
| chr3:123530115
|
GATTAATG others(38): Show |
G | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1686_293-1642d others(47): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530115 | ||||||
| chr3:123530125
|
G | A | 1 | a0001c0003t0003g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.293-1651C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530125 | ||||||
| chr3:123530141
|
C | T | 1 | a0001c0001t0004g0181 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.293-1667G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530141 | ||||||
| chr3:123530167
|
A | T | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1693T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530167 | ||||||
| chr3:123530177
|
A | G | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1703T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530177 | ||||||
| chr3:123530261
|
A | T | 5 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-1787T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530261 | ||||||
| chr3:123530394
|
C | T | 1 | a0001c0003t0003g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.293-1920G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530394 | ||||||
| chr3:123530408
|
A | AT | 101 | a0001c0001t0002g0131a0001c0001t0003g0112a0001c0001t0003g0154others(98): Show | 103 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.293-1935dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530408 | ||||||
| chr3:123530408
|
A | T | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-1934T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530408 | ||||||
| chr3:123530433
|
G | A | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293-1959C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530433 | ||||||
| chr3:123530554
|
A | G | 1 | a0001c0002t0001g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.293-2080T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530554 | ||||||
| chr3:123530615
|
G | A | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.293-2141C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530615 | ||||||
| chr3:123530663
|
T | G | 1 | a0001c0002t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.293-2189A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530663 | ||||||
| chr3:123530696
|
T | A | 107 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(104): Show | 109 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.293-2222A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530696 | ||||||
| chr3:123530702
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-2228G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530702 | ||||||
| chr3:123530781
|
A | G | 92 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(89): Show | 94 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.293-2307T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530781 | ||||||
| chr3:123530862
|
TTTG | T | 3 | a0001c0001t0004g0164a0001c0001t0004g0184a0001c0001t0004g0185 | 3 | NA18949.hp2 NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.293-2391_293-2389d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530862 | ||||||
| chr3:123530895
|
T | G | 1 | a0001c0002t0005g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.293-2421A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530895 | ||||||
| chr3:123530907
|
G | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.293-2433C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530907 | ||||||
| chr3:123531317
|
TTTTTC | T | 109 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.293-2848_293-2844d others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123531317 | ||||||
| chr3:123531406
|
G | A | 1 | a0001c0003t0005g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.293-2932C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123531406 | ||||||
| chr3:123531468
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-2994G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123531468 | ||||||
| chr3:123532075
|
C | G | 14 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0080others(11): Show | 14 | NA18959.hp1 NA18962.hp1 NA18964.hp2 others(11): Show |
intron_variant | MODIFIER | c.293-3601G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532075 | ||||||
| chr3:123532137
|
A | G | 2 | a0001c0001t0002g0193a0001c0003t0003g0006 | 3 | HG01256.hp1 NA18939.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.293-3663T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532137 | ||||||
| chr3:123532150
|
A | G | 2 | a0001c0003t0003g0256a0001c0003t0003g0258 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-3676T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532150 | ||||||
| chr3:123532275
|
C | T | 2 | a0001c0002t0005g0074a0001c0002t0005g0076 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.293-3801G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532275 | ||||||
| chr3:123532391
|
T | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-3917A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532391 | ||||||
| chr3:123532407
|
T | C | 1 | a0001c0002t0001g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.293-3933A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532407 | ||||||
| chr3:123532432
|
G | C | 1 | a0001c0003t0003g0292 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.293-3958C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532432 | ||||||
| chr3:123532435
|
T | G | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.293-3961A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532435 | ||||||
| chr3:123532445
|
A | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293-3971T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532445 | ||||||
| chr3:123532552
|
C | T | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.293-4078G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532552 | ||||||
| chr3:123532566
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-4092A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532566 | ||||||
| chr3:123532569
|
G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-4095C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532569 | ||||||
| chr3:123532670
|
T | A | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.293-4196A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532670 | ||||||
| chr3:123532705
|
A | G | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-4231T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532705 | ||||||
| chr3:123532783
|
G | A | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-4309C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532783 | ||||||
| chr3:123532784
|
A | C | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.293-4310T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532784 | ||||||
| chr3:123532826
|
T | C | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-4352A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532826 | ||||||
| chr3:123532833
|
C | CA | 15 | a0001c0001t0002g0167a0001c0001t0006g0233a0001c0001t0006g0236others(12): Show | 15 | HG01109.hp2 HG02080.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.293-4360dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532833 | ||||||
| chr3:123532833
|
CA | C | 195 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(192): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.293-4360delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532833 | ||||||
| chr3:123532833
|
CAA | C | 10 | a0001c0001t0002g0171a0001c0001t0004g0109a0001c0001t0013g0115others(7): Show | 10 | HG01168.hp1 HG01168.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-4361_293-4360d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532833 | ||||||
| chr3:123532833
|
CAAA | C | 13 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.293-4362_293-4360d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532833 | ||||||
| chr3:123532917
|
T | C | 1 | a0001c0002t0005g0067 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.293-4443A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532917 | ||||||
| chr3:123532946
|
A | G | 25 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.293-4472T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532946 | ||||||
| chr3:123533059
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.293-4585C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533059 | ||||||
| chr3:123533114
|
G | C | 266 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(263): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.293-4640C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533114 | ||||||
| chr3:123533118
|
T | A | 1 | a0001c0002t0001g0029 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.293-4644A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533118 | ||||||
| chr3:123533213
|
ATCATGGC others(11): Show |
A | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-4757_293-4740d others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533213 | ||||||
| chr3:123533321
|
G | A | 1 | a0001c0001t0015g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.293-4847C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533321 | ||||||
| chr3:123533349
|
A | G | 1 | a0001c0003t0005g0301 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.293-4875T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533349 | ||||||
| chr3:123533377
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.293-4903T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533377 | ||||||
| chr3:123533395
|
C | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-4921G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533395 | ||||||
| chr3:123533428
|
C | T | 33 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(30): Show | 33 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.293-4954G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533428 | ||||||
| chr3:123533443
|
T | G | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293-4969A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533443 | ||||||
| chr3:123533800
|
C | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-5326G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533800 | ||||||
| chr3:123534029
|
A | AGT | 225 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(222): Show | 232 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.293-5557_293-5556d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | ||||||
| chr3:123534029
|
A | AGTGT | 36 | a0001c0001t0002g0125a0001c0001t0002g0134a0001c0001t0002g0136others(33): Show | 36 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.293-5559_293-5556d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | ||||||
| chr3:123534029
|
A | AGTGTGT | 31 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(28): Show | 32 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.293-5561_293-5556d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | ||||||
| chr3:123534029
|
A | AGTGTGTG others(1): Show |
5 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-5563_293-5556d others(10): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | ||||||
| chr3:123534029
|
A | AGTGTGTG others(3): Show |
3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.293-5565_293-5556d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | ||||||
| chr3:123534153
|
A | G | 45 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(42): Show | 45 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.293-5679T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534153 | ||||||
| chr3:123534366
|
C | T | 27 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(24): Show | 27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-5892G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534366 | ||||||
| chr3:123534721
|
G | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-6247C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534721 | ||||||
| chr3:123534793
|
T | C | 3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.293-6319A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534793 | ||||||
| chr3:123534798
|
T | TTGTGTGT others(7): Show |
49 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0002t0003g0075others(46): Show | 51 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(48): Show |
intron_variant | MODIFIER | c.293-6338_293-6325d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | ||||||
| chr3:123534798
|
T | TTGTGTGT others(9): Show |
237 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(234): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.293-6325_293-6324i others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | ||||||
| chr3:123534798
|
T | TTGTGTGT others(11): Show |
11 | a0001c0001t0002g0201a0001c0001t0002g0213a0001c0001t0002g0220others(8): Show | 11 | HG01516.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.293-6325_293-6324i others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | ||||||
| chr3:123534798
|
T | TTGTGTGT others(13): Show |
3 | a0001c0001t0013g0115a0001c0003t0014g0298a0001c0003t0014g0299 | 3 | HG02055.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-6325_293-6324i others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | ||||||
| chr3:123534798
|
T | TTGTGTGT others(15): Show |
8 | a0001c0001t0013g0116a0001c0003t0007g0305a0001c0003t0007g0306others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-6325_293-6324i others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | ||||||
| chr3:123534798
|
T | TTGTGTGT others(17): Show |
1 | a0001c0003t0007g0309 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.293-6325_293-6324i others(26): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | ||||||
| chr3:123534798
|
T | TTGTGTGT others(19): Show |
2 | a0001c0003t0010g0337a0001c0003t0010g0338 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.293-6325_293-6324i others(28): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | ||||||
| chr3:123534798
|
T | TTGTGTGT others(23): Show |
2 | a0001c0003t0010g0339a0001c0003t0010g0340 | 2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.293-6325_293-6324i others(32): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | ||||||
| chr3:123534877
|
T | C | 20 | a0001c0001t0002g0117a0001c0001t0002g0122a0001c0001t0002g0123others(17): Show | 20 | HG00423.hp1 HG00558.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.293-6403A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534877 | ||||||
| chr3:123535068
|
G | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-6594C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535068 | ||||||
| chr3:123535219
|
G | A | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-6745C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535219 | ||||||
| chr3:123535264
|
G | A | 1 | a0001c0003t0009g0267 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.293-6790C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535264 | ||||||
| chr3:123535351
|
A | G | 27 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(24): Show | 27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-6877T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535351 | ||||||
| chr3:123535352
|
T | C | 1 | a0001c0002t0001g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.293-6878A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535352 | ||||||
| chr3:123535670
|
G | T | 3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.293-7196C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535670 | ||||||
| chr3:123535752
|
T | C | 328 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(325): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.293-7278A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535752 | ||||||
| chr3:123535763
|
A | G | 1 | a0001c0002t0001g0049 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.293-7289T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535763 | ||||||
| chr3:123535907
|
G | T | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-7433C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535907 | ||||||
| chr3:123535985
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.293-7511A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535985 | ||||||
| chr3:123536186
|
C | T | 3 | a0001c0001t0004g0179a0001c0001t0004g0180a0001c0001t0004g0183 | 3 | HG00642.hp1 HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.293-7712G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536186 | ||||||
| chr3:123536281
|
G | A | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-7807C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536281 | ||||||
| chr3:123536326
|
G | A | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-7852C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536326 | ||||||
| chr3:123536515
|
C | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-8041G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536515 | ||||||
| chr3:123536640
|
A | G | 1 | a0001c0003t0024g0326 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.293-8166T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536640 | ||||||
| chr3:123536649
|
G | T | 1 | a0001c0003t0001g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.293-8175C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536649 | ||||||
| chr3:123536651
|
C | T | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-8177G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536651 | ||||||
| chr3:123536756
|
A | G | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-8282T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536756 | ||||||
| chr3:123536896
|
G | A | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-8422C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536896 | ||||||
| chr3:123536908
|
C | T | 4 | a0001c0002t0004g0002a0001c0002t0004g0099a0001c0002t0004g0102others(1): Show | 5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-8434G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536908 | ||||||
| chr3:123536930
|
G | A | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.293-8456C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536930 | ||||||
| chr3:123536996
|
G | A | 4 | a0001c0003t0003g0260a0001c0003t0003g0263a0001c0003t0003g0271others(1): Show | 4 | HG02080.hp2 HG02083.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-8522C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536996 | ||||||
| chr3:123537042
|
T | C | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | NA18966.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.293-8568A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537042 | ||||||
| chr3:123537074
|
A | G | 8 | a0001c0002t0001g0015a0001c0002t0001g0081a0001c0002t0001g0082others(5): Show | 8 | NA18962.hp1 NA18972.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-8600T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537074 | ||||||
| chr3:123537108
|
A | G | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-8634T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537108 | ||||||
| chr3:123537110
|
A | G | 3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.293-8636T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537110 | ||||||
| chr3:123537279
|
A | C | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.293-8805T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537279 | ||||||
| chr3:123537329
|
A | G | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-8855T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537329 | ||||||
| chr3:123537331
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.293-8857G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537331 | ||||||
| chr3:123537418
|
A | T | 4 | a0001c0001t0006g0238a0001c0001t0006g0241a0001c0001t0006g0245others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-8944T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537418 | ||||||
| chr3:123537556
|
C | T | 221 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(218): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.293-9082G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537556 | ||||||
| chr3:123537576
|
AATACAC | A | 11 | a0001c0001t0005g0139a0001c0001t0005g0173a0001c0002t0005g0020others(8): Show | 11 | HG00673.hp2 HG01109.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.293-9108_293-9103d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537576 | ||||||
| chr3:123537578
|
T | TAC | 74 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0002g0161others(71): Show | 77 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.293-9106_293-9105d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | ||||||
| chr3:123537578
|
T | TACAC | 16 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0222others(13): Show | 16 | HG01884.hp2 HG01928.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-9108_293-9105d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | ||||||
| chr3:123537578
|
T | TACACACA others(3): Show |
1 | a0001c0003t0014g0299 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.293-9105_293-9104i others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | ||||||
| chr3:123537578
|
T | TACACACA others(7): Show |
1 | a0001c0003t0007g0305 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.293-9105_293-9104i others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | ||||||
| chr3:123537578
|
T | TACACACA others(9): Show |
7 | a0001c0003t0007g0306a0001c0003t0007g0307a0001c0003t0007g0308others(4): Show | 7 | HG00099.hp1 HG00642.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-9105_293-9104i others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | ||||||
| chr3:123537578
|
TACACATA others(3): Show |
T | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-9114_293-9105d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | ||||||
| chr3:123537580
|
CACAT | C | 16 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0199others(13): Show | 16 | HG00639.hp2 HG00738.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-9110_293-9107d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537580 | ||||||
| chr3:123537582
|
CAT | C | 20 | a0001c0001t0006g0219a0001c0001t0006g0225a0001c0001t0006g0226others(17): Show | 20 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-9110_293-9109d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537582 | ||||||
| chr3:123537584
|
T | C | 233 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(230): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.293-9110A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537584 | ||||||
| chr3:123537627
|
A | T | 1 | a0001c0003t0003g0285 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.293-9153T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537627 | ||||||
| chr3:123537630
|
AT | A | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-9157delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537630 | ||||||
| chr3:123537884
|
AATC | A | 27 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(24): Show | 27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-9413_293-9411d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537884 | ||||||
| chr3:123537921
|
T | C | 2 | a0001c0003t0007g0307a0001c0003t0007g0308 | 2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.293-9447A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537921 | ||||||
| chr3:123537963
|
A | C | 2 | a0001c0003t0007g0307a0001c0003t0007g0308 | 2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.293-9489T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537963 | ||||||
| chr3:123538053
|
A | G | 1 | a0001c0001t0006g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.293-9579T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538053 | ||||||
| chr3:123538218
|
T | C | 4 | a0001c0002t0004g0002a0001c0002t0004g0099a0001c0002t0004g0102others(1): Show | 5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-9744A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538218 | ||||||
| chr3:123538258
|
T | C | 109 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.293-9784A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538258 | ||||||
| chr3:123538623
|
A | G | 1 | a0001c0001t0006g0250 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293-10149T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538623 | ||||||
| chr3:123538635
|
C | T | 2 | a0001c0001t0002g0128a0001c0001t0002g0132 | 2 | HG02071.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.293-10161G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538635 | ||||||
| chr3:123538666
|
T | C | 109 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0108others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.293-10192A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538666 | ||||||
| chr3:123538747
|
C | T | 1 | a0001c0002t0001g0049 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.293-10273G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538747 | ||||||
| chr3:123538862
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0135 | 3 | HG01346.hp2 HG01358.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.293-10388C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538862 | ||||||
| chr3:123539154
|
T | C | 221 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(218): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.293-10680A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539154 | ||||||
| chr3:123539364
|
G | A | 71 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(68): Show | 72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.293-10890C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539364 | ||||||
| chr3:123539493
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.293-11019G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539493 | ||||||
| chr3:123539513
|
T | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0145 | 3 | NA18994.hp1 NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.293-11039A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539513 | ||||||
| chr3:123539564
|
G | T | 1 | a0001c0002t0001g0022 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.293-11090C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539564 | ||||||
| chr3:123539613
|
C | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293-11139G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539613 | ||||||
| chr3:123539911
|
T | TA | 32 | a0001c0001t0002g0251a0001c0001t0006g0218a0001c0001t0006g0219others(29): Show | 32 | HG00099.hp1 HG00642.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.293-11438dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
T | TAA | 57 | a0001c0001t0004g0203a0001c0001t0006g0226a0001c0001t0009g0138others(54): Show | 58 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.293-11439_293-1143 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
T | TAAA | 68 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(65): Show | 69 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.293-11440_293-1143 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
T | TAAAA | 55 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(52): Show | 58 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.293-11441_293-1143 others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
T | TAAAAA | 18 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0127others(15): Show | 18 | HG00423.hp1 HG00544.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.293-11442_293-1143 others(9): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
T | TAAAAAA | 9 | a0001c0001t0002g0172a0001c0001t0002g0174a0001c0001t0002g0191others(6): Show | 9 | HG00140.hp1 HG01071.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.293-11443_293-1143 others(10): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
T | TAAAAAAA others(1): Show |
8 | a0001c0001t0002g0005a0001c0003t0003g0327a0001c0003t0003g0329others(5): Show | 9 | HG01070.hp2 HG01081.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-11445_293-1143 others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
T | TAAAAAAA others(3): Show |
1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.293-11447_293-1143 others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
TA | T | 25 | a0001c0001t0003g0154a0001c0001t0015g0223a0001c0001t0015g0224others(22): Show | 27 | HG00639.hp2 HG01109.hp1 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-11438delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123539911
|
TAAAAAAA others(3): Show |
T | 4 | a0001c0002t0001g0081a0001c0002t0001g0082a0001c0002t0001g0084others(1): Show | 4 | NA18982.hp2 NA19002.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-11447_293-1143 others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | ||||||
| chr3:123540007
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.293-11533C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540007 | ||||||
| chr3:123540235
|
C | T | 45 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(42): Show | 45 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.293-11761G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540235 | ||||||
| chr3:123540423
|
T | C | 1 | a0001c0001t0006g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.293-11949A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540423 | ||||||
| chr3:123540490
|
A | G | 1 | a0001c0001t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.293-12016T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540490 | ||||||
| chr3:123540492
|
G | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0024a0001c0002t0001g0050others(1): Show | 4 | NA18973.hp2 NA18983.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-12018C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540492 | ||||||
| chr3:123540512
|
C | T | 5 | a0001c0002t0001g0010a0001c0002t0001g0059a0001c0002t0001g0060others(2): Show | 5 | HG01123.hp2 HG01255.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-12038G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540512 | ||||||
| chr3:123540513
|
G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-12039C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540513 | ||||||
| chr3:123540569
|
G | A | 3 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0340 | 3 | HG02451.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.293-12095C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540569 | ||||||
| chr3:123540578
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.293-12104A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540578 | ||||||
| chr3:123540591
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.293-12117T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540591 | ||||||
| chr3:123540633
|
G | T | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-12159C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540633 | ||||||
| chr3:123540677
|
T | C | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-12203A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540677 | ||||||
| chr3:123540855
|
A | G | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-12381T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540855 | ||||||
| chr3:123541055
|
G | A | 2 | a0001c0001t0006g0233a0001c0001t0006g0242 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.293-12581C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541055 | ||||||
| chr3:123541145
|
C | T | 1 | a0001c0002t0022g0018 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.293-12671G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541145 | ||||||
| chr3:123541243
|
A | C | 339 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(336): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.293-12769T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541243 | ||||||
| chr3:123541292
|
T | C | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.293-12818A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541292 | ||||||
| chr3:123541697
|
T | G | 1 | a0001c0001t0004g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.293-13223A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541697 | ||||||
| chr3:123541837
|
A | G | 1 | a0001c0001t0006g0225 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.293-13363T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541837 | ||||||
| chr3:123541918
|
C | T | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-13444G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541918 | ||||||
| chr3:123541953
|
C | T | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-13479G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541953 | ||||||
| chr3:123542019
|
C | T | 1 | a0001c0003t0001g0324 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.293-13545G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542019 | ||||||
| chr3:123542126
|
G | A | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-13652C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542126 | ||||||
| chr3:123542142
|
G | A | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-13668C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542142 | ||||||
| chr3:123542146
|
C | CA | 188 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(185): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.293-13673dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAA | 18 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(15): Show | 18 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.293-13674_293-1367 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAA | 47 | a0001c0001t0001g0222a0001c0001t0003g0112a0001c0001t0003g0154others(44): Show | 49 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(46): Show |
intron_variant | MODIFIER | c.293-13675_293-1367 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0005g0020 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.293-13683_293-1367 others(15): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0005g0021 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.293-13685_293-1367 others(17): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(7): Show |
2 | a0001c0002t0005g0096a0001c0002t0005g0097 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.293-13686_293-1367 others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(8): Show |
2 | a0001c0002t0005g0094a0001c0002t0005g0095 | 2 | HG01433.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.293-13687_293-1367 others(19): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.293-13688_293-1367 others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(10): Show |
1 | a0001c0002t0005g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.293-13689_293-1367 others(21): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(11): Show |
1 | a0001c0002t0005g0064 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.293-13690_293-1367 others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0005g0113a0001c0001t0005g0173 | 2 | HG01358.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.293-13691_293-1367 others(23): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0005g0114a0001c0002t0005g0066a0001c0002t0005g0079 | 3 | HG01361.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.293-13692_293-1367 others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(14): Show |
2 | a0001c0002t0005g0068a0001c0002t0005g0069 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.293-13693_293-1367 others(25): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(16): Show |
1 | a0001c0002t0005g0073 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293-13695_293-1367 others(27): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(18): Show |
4 | a0001c0001t0005g0139a0001c0001t0005g0200a0001c0002t0005g0067others(1): Show | 4 | HG00673.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-13697_293-1367 others(29): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
C | CAAAAAAA others(20): Show |
1 | a0001c0002t0005g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.293-13673_293-1367 others(31): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542146
|
CAAA | C | 10 | a0001c0001t0013g0115a0001c0003t0007g0305a0001c0003t0007g0307others(7): Show | 10 | HG00642.hp2 HG00735.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-13675_293-1367 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | ||||||
| chr3:123542165
|
A | AG | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-13692_293-1369 others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542165 | ||||||
| chr3:123542194
|
T | A | 314 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(311): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.293-13720A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542194 | ||||||
| chr3:123542223
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.293-13749C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542223 | ||||||
| chr3:123542435
|
A | G | 318 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(315): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.293-13961T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542435 | ||||||
| chr3:123542543
|
C | T | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-14069G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542543 | ||||||
| chr3:123542666
|
A | T | 5 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-14192T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542666 | ||||||
| chr3:123542778
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-14304G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542778 | ||||||
| chr3:123542959
|
T | C | 1 | a0001c0003t0005g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.293-14485A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542959 | ||||||
| chr3:123543121
|
C | T | 117 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(114): Show | 118 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.293-14647G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543121 | ||||||
| chr3:123543189
|
T | C | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-14715A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543189 | ||||||
| chr3:123543349
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-14875T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543349 | ||||||
| chr3:123543420
|
CA | C | 27 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(24): Show | 27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-14947delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543420 | ||||||
| chr3:123543509
|
C | A | 2 | a0001c0002t0005g0074a0001c0002t0005g0076 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.293-15035G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543509 | ||||||
| chr3:123543513
|
G | A | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-15039C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543513 | ||||||
| chr3:123543807
|
C | CT | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-15334dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543807 | ||||||
| chr3:123544018
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.293-15544T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544018 | ||||||
| chr3:123544100
|
C | T | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-15626G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544100 | ||||||
| chr3:123544112
|
G | A | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-15638C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544112 | ||||||
| chr3:123544272
|
A | G | 13 | a0001c0001t0006g0233a0001c0001t0006g0234a0001c0001t0006g0235others(10): Show | 13 | HG02109.hp2 HG02572.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-15798T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544272 | ||||||
| chr3:123544394
|
C | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG00738.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.293-15920G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544394 | ||||||
| chr3:123544394
|
C | T | 38 | a0001c0001t0002g0182a0001c0001t0004g0004a0001c0001t0004g0109others(35): Show | 40 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.293-15920G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544394 | ||||||
| chr3:123544408
|
G | T | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.293-15934C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544408 | ||||||
| chr3:123544435
|
T | A | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-15961A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544435 | ||||||
| chr3:123544559
|
A | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-16085T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544559 | ||||||
| chr3:123544617
|
T | C | 4 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-16143A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544617 | ||||||
| chr3:123544742
|
T | C | 75 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0006g0218others(72): Show | 77 | HG00544.hp2 HG01109.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.293-16268A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544742 | ||||||
| chr3:123544766
|
TA | T | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-16293delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544766 | ||||||
| chr3:123544986
|
A | G | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-16512T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544986 | ||||||
| chr3:123545007
|
G | A | 1 | a0001c0002t0005g0073 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293-16533C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545007 | ||||||
| chr3:123545034
|
C | CA | 139 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(136): Show | 142 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.293-16561dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545034 | ||||||
| chr3:123545034
|
C | CAA | 25 | a0001c0001t0003g0112a0001c0002t0001g0017a0001c0002t0001g0039others(22): Show | 26 | HG00423.hp2 HG00544.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.293-16562_293-1656 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545034 | ||||||
| chr3:123545034
|
CA | C | 16 | a0001c0001t0002g0120a0001c0001t0004g0175a0001c0001t0004g0206others(13): Show | 16 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-16561delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545034 | ||||||
| chr3:123545099
|
G | T | 2 | a0001c0001t0005g0113a0001c0001t0005g0114 | 2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.293-16625C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545099 | ||||||
| chr3:123545139
|
G | GT | 42 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(39): Show | 42 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.293-16666dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545139 | ||||||
| chr3:123545139
|
GT | G | 10 | a0001c0001t0002g0220a0001c0001t0015g0223a0001c0001t0015g0224others(7): Show | 10 | HG00597.hp2 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-16666delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545139 | ||||||
| chr3:123545170
|
T | C | 80 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(77): Show | 81 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.293-16696A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545170 | ||||||
| chr3:123545286
|
C | G | 45 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(42): Show | 45 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.293-16812G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545286 | ||||||
| chr3:123545363
|
T | C | 3 | a0001c0001t0006g0234a0001c0001t0006g0235a0001c0001t0006g0236 | 3 | HG02976.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.293-16889A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545363 | ||||||
| chr3:123545376
|
G | A | 3 | a0001c0003t0003g0253a0001c0003t0003g0283a0001c0003t0003g0284 | 3 | NA19000.hp2 NA19002.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.293-16902C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545376 | ||||||
| chr3:123545460
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.293-16986G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545460 | ||||||
| chr3:123545486
|
A | AAAAT | 10 | a0001c0001t0002g0159a0001c0001t0002g0251a0001c0001t0006g0233others(7): Show | 10 | HG00642.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-17016_293-1701 others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | ||||||
| chr3:123545486
|
A | AAAATAAA others(1): Show |
75 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0006g0218others(72): Show | 77 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.293-17020_293-1701 others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | ||||||
| chr3:123545486
|
A | AAAATAAA others(5): Show |
23 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(20): Show | 23 | HG00099.hp1 HG00673.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-17024_293-1701 others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | ||||||
| chr3:123545486
|
A | AAAATAAA others(9): Show |
7 | a0001c0001t0005g0173a0001c0001t0005g0199a0001c0001t0005g0200others(4): Show | 7 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-17028_293-1701 others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | ||||||
| chr3:123545486
|
A | AAAATAAA others(13): Show |
2 | a0001c0002t0005g0094a0001c0002t0005g0096 | 2 | HG01433.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.293-17032_293-1701 others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | ||||||
| chr3:123545486
|
AAAAT | A | 210 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(207): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.293-17016_293-1701 others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | ||||||
| chr3:123545486
|
AAAATAAA others(5): Show |
A | 1 | a0001c0002t0001g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.293-17024_293-1701 others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | ||||||
| chr3:123545490
|
T | TAAATAAA others(10910): Show |
1 | a0001c0002t0008g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.293-17017_293-1701 others(10921): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545490 | ||||||
| chr3:123545548
|
T | TA | 9 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0001g0325others(6): Show | 9 | HG00544.hp2 HG02965.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.293-17075dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545548 | ||||||
| chr3:123545548
|
TA | T | 51 | a0001c0001t0002g0118a0001c0001t0002g0193a0001c0001t0002g0198others(48): Show | 52 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.293-17075delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545548 | ||||||
| chr3:123545647
|
A | G | 1 | a0001c0002t0005g0067 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.293-17173T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545647 | ||||||
| chr3:123545690
|
C | A | 33 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(30): Show | 33 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.293-17216G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545690 | ||||||
| chr3:123545713
|
A | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-17239T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545713 | ||||||
| chr3:123545715
|
A | AT | 7 | a0001c0001t0002g0155a0001c0001t0002g0182a0001c0001t0002g0215others(4): Show | 7 | HG01515.hp2 HG02155.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-17242dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545715 | ||||||
| chr3:123546251
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.293-17777A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546251 | ||||||
| chr3:123546267
|
G | A | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-17793C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546267 | ||||||
| chr3:123546308
|
G | A | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-17834C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546308 | ||||||
| chr3:123546484
|
C | G | 15 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0040others(12): Show | 16 | HG00558.hp2 HG00673.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-18010G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546484 | ||||||
| chr3:123546569
|
G | A | 1 | a0001c0001t0002g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.293-18095C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546569 | ||||||
| chr3:123546775
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-18301G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546775 | ||||||
| chr3:123546928
|
A | G | 4 | a0001c0002t0004g0002a0001c0002t0004g0099a0001c0002t0004g0102others(1): Show | 5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-18454T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546928 | ||||||
| chr3:123546977
|
T | C | 162 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(159): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.293-18503A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546977 | ||||||
| chr3:123547023
|
C | G | 3 | a0001c0001t0004g0147a0001c0001t0004g0175a0001c0001t0004g0190 | 3 | HG01257.hp2 HG02602.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.293-18549G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547023 | ||||||
| chr3:123547063
|
AT | A | 3 | a0001c0002t0005g0068a0001c0002t0005g0069a0001c0002t0005g0073 | 3 | HG02970.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.293-18590delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547063 | ||||||
| chr3:123547233
|
T | C | 116 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(113): Show | 119 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.293-18759A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547233 | ||||||
| chr3:123547510
|
G | A | 24 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(21): Show | 24 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-19036C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547510 | ||||||
| chr3:123547803
|
C | T | 228 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(225): Show | 232 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.293-19329G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547803 | ||||||
| chr3:123547904
|
C | T | 1 | a0001c0003t0001g0314 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.293-19430G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547904 | ||||||
| chr3:123547986
|
C | G | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-19512G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547986 | ||||||
| chr3:123548092
|
G | A | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-19618C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548092 | ||||||
| chr3:123548211
|
A | G | 1 | a0001c0002t0001g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.292+19551T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548211 | ||||||
| chr3:123548250
|
T | C | 80 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(77): Show | 81 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.292+19512A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548250 | ||||||
| chr3:123548338
|
C | T | 71 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(68): Show | 72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.292+19424G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548338 | ||||||
| chr3:123548417
|
A | G | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+19345T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548417 | ||||||
| chr3:123548428
|
C | T | 2 | a0001c0003t0001g0008a0001c0003t0001g0319 | 3 | HG00140.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.292+19334G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548428 | ||||||
| chr3:123548556
|
T | C | 75 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0006g0218others(72): Show | 77 | HG00544.hp2 HG01109.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.292+19206A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548556 | ||||||
| chr3:123548644
|
A | G | 1 | a0001c0002t0005g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.292+19118T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548644 | ||||||
| chr3:123548740
|
G | T | 1 | a0001c0003t0003g0270 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.292+19022C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548740 | ||||||
| chr3:123548821
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.292+18941G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548821 | ||||||
| chr3:123548826
|
T | C | 4 | a0001c0002t0001g0011a0001c0002t0001g0026a0001c0002t0001g0027others(1): Show | 4 | HG00597.hp2 NA18946.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+18936A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548826 | ||||||
| chr3:123548833
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+18929G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548833 | ||||||
| chr3:123548892
|
T | A | 1 | a0001c0001t0002g0131 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.292+18870A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548892 | ||||||
| chr3:123549009
|
A | G | 229 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(226): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.292+18753T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549009 | ||||||
| chr3:123549181
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.292+18581G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549181 | ||||||
| chr3:123549184
|
T | C | 1 | a0001c0001t0027g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.292+18578A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549184 | ||||||
| chr3:123549295
|
A | C | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+18467T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549295 | ||||||
| chr3:123549391
|
G | A | 170 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(167): Show | 172 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.292+18371C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549391 | ||||||
| chr3:123549426
|
G | A | 23 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(20): Show | 23 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.292+18336C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549426 | ||||||
| chr3:123549500
|
C | A | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.292+18262G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549500 | ||||||
| chr3:123549542
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.292+18220C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549542 | ||||||
| chr3:123549653
|
T | C | 1 | a0001c0003t0003g0291 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.292+18109A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549653 | ||||||
| chr3:123549661
|
T | C | 5 | a0001c0002t0005g0094a0001c0002t0005g0095a0001c0002t0005g0096others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+18101A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549661 | ||||||
| chr3:123549663
|
G | T | 27 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0225others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+18099C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549663 | ||||||
| chr3:123549672
|
T | C | 2 | a0001c0003t0003g0320a0001c0003t0005g0301 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.292+18090A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549672 | ||||||
| chr3:123549686
|
T | A | 1 | a0001c0002t0001g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.292+18076A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549686 | ||||||
| chr3:123549751
|
AAAC | A | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.292+18008_292+1801 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549751 | ||||||
| chr3:123549866
|
TGGGG | T | 4 | a0001c0001t0004g0205a0001c0001t0004g0209a0001c0001t0004g0212others(1): Show | 4 | HG00639.hp1 HG01978.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+17892_292+1789 others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549866 | ||||||
| chr3:123549885
|
A | C | 5 | a0001c0003t0003g0264a0001c0003t0003g0265a0001c0003t0003g0268others(2): Show | 5 | HG01928.hp2 HG01943.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+17877T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549885 | ||||||
| chr3:123550086
|
A | C | 27 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0225others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+17676T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550086 | ||||||
| chr3:123550120
|
G | A | 27 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0225others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+17642C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550120 | ||||||
| chr3:123550149
|
A | C | 2 | a0001c0001t0004g0202a0001c0001t0004g0204 | 2 | HG00099.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.292+17613T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550149 | ||||||
| chr3:123550154
|
C | A | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+17608G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550154 | ||||||
| chr3:123550236
|
C | G | 75 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0006g0218others(72): Show | 77 | HG00544.hp2 HG01109.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.292+17526G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550236 | ||||||
| chr3:123550289
|
T | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0057 | 2 | NA18944.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.292+17473A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550289 | ||||||
| chr3:123550293
|
C | T | 9 | a0001c0001t0015g0224a0001c0003t0007g0305a0001c0003t0007g0306others(6): Show | 9 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+17469G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550293 | ||||||
| chr3:123550315
|
G | A | 1 | a0001c0001t0006g0250 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.292+17447C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550315 | ||||||
| chr3:123550667
|
C | A | 1 | a0001c0003t0012g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+17095G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550667 | ||||||
| chr3:123550686
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.292+17076C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550686 | ||||||
| chr3:123550836
|
T | C | 4 | a0001c0002t0001g0029a0001c0002t0001g0037a0001c0002t0001g0038others(1): Show | 4 | HG00423.hp2 HG02027.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+16926A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550836 | ||||||
| chr3:123550866
|
G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292+16896C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550866 | ||||||
| chr3:123550925
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.292+16837A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550925 | ||||||
| chr3:123550977
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.292+16785C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550977 | ||||||
| chr3:123551127
|
G | A | 4 | a0001c0002t0001g0011a0001c0002t0001g0026a0001c0002t0001g0027others(1): Show | 4 | HG00597.hp2 NA18946.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+16635C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551127 | ||||||
| chr3:123551265
|
A | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+16497T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551265 | ||||||
| chr3:123551311
|
T | C | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+16451A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551311 | ||||||
| chr3:123551346
|
C | T | 2 | a0001c0002t0001g0030a0001c0002t0001g0049 | 2 | HG04115.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.292+16416G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551346 | ||||||
| chr3:123551424
|
G | A | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.292+16338C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551424 | ||||||
| chr3:123551456
|
T | TA | 5 | a0001c0001t0005g0139a0001c0002t0005g0020a0001c0002t0005g0021others(2): Show | 5 | HG00673.hp2 NA18994.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+16305dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551456 | ||||||
| chr3:123551464
|
A | T | 85 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(82): Show | 88 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.292+16298T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551464 | ||||||
| chr3:123551494
|
G | A | 3 | a0001c0003t0003g0289a0001c0003t0003g0334a0001c0003t0003g0335 | 3 | HG02071.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.292+16268C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551494 | ||||||
| chr3:123551599
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | NA18966.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.292+16163C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551599 | ||||||
| chr3:123551917
|
A | C | 1 | a0001c0001t0002g0129 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.292+15845T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551917 | ||||||
| chr3:123552085
|
T | C | 1 | a0001c0001t0006g0244 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.292+15677A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552085 | ||||||
| chr3:123552238
|
C | T | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+15524G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552238 | ||||||
| chr3:123552245
|
C | A | 87 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.292+15517G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552245 | ||||||
| chr3:123552837
|
A | G | 131 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.292+14925T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552837 | ||||||
| chr3:123552960
|
G | A | 1 | a0001c0002t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.292+14802C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552960 | ||||||
| chr3:123553114
|
T | C | 1 | a0001c0003t0003g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292+14648A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553114 | ||||||
| chr3:123553244
|
G | C | 1 | a0001c0001t0002g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.292+14518C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553244 | ||||||
| chr3:123553449
|
A | G | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+14313T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553449 | ||||||
| chr3:123553517
|
T | C | 2 | a0001c0001t0002g0128a0001c0001t0002g0132 | 2 | HG02071.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.292+14245A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553517 | ||||||
| chr3:123553571
|
G | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.292+14191C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553571 | ||||||
| chr3:123553952
|
T | A | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+13810A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553952 | ||||||
| chr3:123553960
|
A | T | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+13802T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553960 | ||||||
| chr3:123554076
|
C | T | 17 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.292+13686G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554076 | ||||||
| chr3:123554134
|
A | AAAGAATA others(135): Show |
340 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(337): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.292+13627_292+1362 others(146): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554134 | ||||||
| chr3:123554134
|
A | AAAGAATA others(135): Show |
1 | a0001c0003t0003g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.292+13627_292+1362 others(146): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554134 | ||||||
| chr3:123554335
|
G | T | 34 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(31): Show | 34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+13427C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554335 | ||||||
| chr3:123554490
|
C | T | 2 | a0001c0002t0001g0012a0001c0002t0001g0048 | 2 | HG02738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.292+13272G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554490 | ||||||
| chr3:123554687
|
C | T | 1 | a0001c0003t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.292+13075G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554687 | ||||||
| chr3:123554798
|
G | A | 1 | a0001c0001t0006g0231 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292+12964C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554798 | ||||||
| chr3:123554828
|
AT | A | 27 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0225others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+12933delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554828 | ||||||
| chr3:123554987
|
C | T | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+12775G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554987 | ||||||
| chr3:123555087
|
T | C | 34 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(31): Show | 34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+12675A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555087 | ||||||
| chr3:123555139
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.292+12623C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555139 | ||||||
| chr3:123555167
|
G | A | 1 | a0001c0002t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.292+12595C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555167 | ||||||
| chr3:123555377
|
C | T | 1 | a0001c0002t0001g0043 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.292+12385G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555377 | ||||||
| chr3:123555431
|
A | G | 34 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(31): Show | 34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+12331T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555431 | ||||||
| chr3:123555476
|
T | TA | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+12285dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555476 | ||||||
| chr3:123555611
|
T | A | 2 | a0001c0003t0003g0329a0001c0003t0003g0336 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+12151A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555611 | ||||||
| chr3:123556006
|
A | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0081a0001c0002t0001g0082others(4): Show | 7 | NA18962.hp1 NA18972.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+11756T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556006 | ||||||
| chr3:123556232
|
T | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+11530A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556232 | ||||||
| chr3:123556320
|
C | G | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.292+11442G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556320 | ||||||
| chr3:123556332
|
G | T | 75 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(72): Show | 76 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.292+11430C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556332 | ||||||
| chr3:123556363
|
G | T | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.292+11399C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556363 | ||||||
| chr3:123556381
|
G | A | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.292+11381C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556381 | ||||||
| chr3:123556425
|
A | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+11337T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556425 | ||||||
| chr3:123556436
|
C | CA | 7 | a0001c0001t0004g0164a0001c0001t0004g0184a0001c0001t0004g0185others(4): Show | 7 | HG01884.hp1 HG02647.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+11325dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556436 | ||||||
| chr3:123556436
|
CA | C | 203 | a0001c0001t0001g0248a0001c0001t0002g0117a0001c0001t0002g0124others(200): Show | 206 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.292+11325delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556436 | ||||||
| chr3:123556453
|
T | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+11309A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556453 | ||||||
| chr3:123556539
|
C | A | 5 | a0001c0002t0005g0094a0001c0002t0005g0095a0001c0002t0005g0096others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+11223G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556539 | ||||||
| chr3:123556551
|
A | G | 73 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(70): Show | 74 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.292+11211T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556551 | ||||||
| chr3:123556875
|
T | C | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.292+10887A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556875 | ||||||
| chr3:123556938
|
C | T | 2 | a0001c0001t0005g0113a0001c0001t0005g0114 | 2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.292+10824G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556938 | ||||||
| chr3:123557011
|
T | A | 3 | a0001c0003t0011g0322a0001c0003t0011g0323a0001c0003t0016g0321 | 3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.292+10751A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557011 | ||||||
| chr3:123557112
|
CGCA | C | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+10647_292+1064 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557112 | ||||||
| chr3:123557310
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.292+10452G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557310 | ||||||
| chr3:123557388
|
C | T | 12 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0003t0007g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+10374G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557388 | ||||||
| chr3:123557667
|
A | G | 1 | a0001c0003t0011g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292+10095T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557667 | ||||||
| chr3:123557713
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.292+10049C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557713 | ||||||
| chr3:123557756
|
C | G | 1 | a0001c0002t0005g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.292+10006G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557756 | ||||||
| chr3:123557869
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.292+9893G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557869 | ||||||
| chr3:123558166
|
G | A | 5 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+9596C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558166 | ||||||
| chr3:123558169
|
G | A | 1 | a0001c0001t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.292+9593C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558169 | ||||||
| chr3:123558233
|
G | A | 1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+9529C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558233 | ||||||
| chr3:123558508
|
G | A | 37 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(34): Show | 38 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.292+9254C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558508 | ||||||
| chr3:123558702
|
T | C | 9 | a0001c0001t0002g0005a0001c0001t0002g0171a0001c0001t0002g0172others(6): Show | 10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+9060A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558702 | ||||||
| chr3:123558849
|
C | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.292+8913G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558849 | ||||||
| chr3:123558972
|
G | C | 240 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(237): Show | 244 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.292+8790C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558972 | ||||||
| chr3:123559073
|
C | T | 1 | a0001c0002t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.292+8689G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559073 | ||||||
| chr3:123559094
|
C | G | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.292+8668G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559094 | ||||||
| chr3:123559183
|
T | G | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+8579A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559183 | ||||||
| chr3:123559253
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.292+8509C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559253 | ||||||
| chr3:123559285
|
GTGT | G | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+8474_292+8476d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559285 | ||||||
| chr3:123559540
|
G | A | 1 | a0001c0003t0012g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+8222C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559540 | ||||||
| chr3:123559552
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.292+8210T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559552 | ||||||
| chr3:123559750
|
C | T | 10 | a0001c0001t0006g0219a0001c0001t0006g0225a0001c0001t0006g0226others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+8012G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559750 | ||||||
| chr3:123559845
|
G | A | 34 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(31): Show | 34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+7917C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559845 | ||||||
| chr3:123560048
|
C | G | 341 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(338): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.292+7714G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560048 | ||||||
| chr3:123560143
|
G | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+7619C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560143 | ||||||
| chr3:123560180
|
G | A | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+7582C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560180 | ||||||
| chr3:123560234
|
G | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+7528C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560234 | ||||||
| chr3:123560255
|
G | T | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292+7507C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560255 | ||||||
| chr3:123560377
|
G | A | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+7385C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560377 | ||||||
| chr3:123560417
|
A | G | 1 | a0001c0002t0001g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.292+7345T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560417 | ||||||
| chr3:123560679
|
C | G | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+7083G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560679 | ||||||
| chr3:123560786
|
CT | C | 72 | a0001c0001t0009g0138a0001c0002t0001g0001a0001c0002t0001g0009others(69): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.292+6975delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560786 | ||||||
| chr3:123560873
|
G | A | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+6889C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560873 | ||||||
| chr3:123560876
|
G | A | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+6886C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560876 | ||||||
| chr3:123561040
|
A | G | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+6722T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561040 | ||||||
| chr3:123561079
|
G | T | 1 | a0001c0001t0002g0159 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.292+6683C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561079 | ||||||
| chr3:123561081
|
G | C | 1 | a0001c0001t0006g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292+6681C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561081 | ||||||
| chr3:123561129
|
C | G | 27 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0225others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+6633G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561129 | ||||||
| chr3:123561167
|
G | A | 2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | HG01168.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.292+6595C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561167 | ||||||
| chr3:123561226
|
T | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+6536A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561226 | ||||||
| chr3:123561254
|
G | A | 162 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(159): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.292+6508C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561254 | ||||||
| chr3:123561315
|
C | T | 1 | a0001c0001t0025g0140 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.292+6447G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561315 | ||||||
| chr3:123561316
|
T | C | 1 | a0001c0001t0025g0140 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.292+6446A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561316 | ||||||
| chr3:123561412
|
G | A | 1 | a0001c0003t0003g0297 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.292+6350C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561412 | ||||||
| chr3:123561488
|
A | G | 1 | a0001c0002t0005g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.292+6274T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561488 | ||||||
| chr3:123561551
|
T | TCACATCT others(21): Show |
2 | a0001c0002t0001g0023a0001c0002t0001g0042 | 2 | HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.292+6183_292+6210d others(30): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561551 | ||||||
| chr3:123561602
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+6160G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561602 | ||||||
| chr3:123561613
|
A | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+6149T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561613 | ||||||
| chr3:123561614
|
G | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+6148C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561614 | ||||||
| chr3:123561689
|
C | G | 1 | a0001c0002t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.292+6073G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561689 | ||||||
| chr3:123561776
|
C | T | 2 | a0001c0001t0015g0223a0001c0001t0015g0224 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.292+5986G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561776 | ||||||
| chr3:123561777
|
G | A | 9 | a0001c0003t0003g0327a0001c0003t0003g0329a0001c0003t0003g0330others(6): Show | 9 | HG02280.hp1 HG02486.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+5985C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561777 | ||||||
| chr3:123561778
|
G | A | 1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+5984C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561778 | ||||||
| chr3:123561778
|
G | GA | 19 | a0001c0001t0002g0132a0001c0001t0002g0145a0001c0001t0002g0157others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.292+5983dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561778 | ||||||
| chr3:123561779
|
A | G | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+5983T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561779 | ||||||
| chr3:123561791
|
A | C | 37 | a0001c0001t0002g0182a0001c0001t0004g0004a0001c0001t0004g0109others(34): Show | 39 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.292+5971T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561791 | ||||||
| chr3:123561864
|
T | C | 1 | a0001c0001t0004g0178 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.292+5898A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561864 | ||||||
| chr3:123561881
|
G | A | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.292+5881C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561881 | ||||||
| chr3:123561905
|
G | A | 27 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0225others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+5857C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561905 | ||||||
| chr3:123561959
|
C | G | 1 | a0001c0001t0002g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.292+5803G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561959 | ||||||
| chr3:123561984
|
G | A | 1 | a0001c0001t0029g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.292+5778C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561984 | ||||||
| chr3:123562091
|
T | A | 1 | a0001c0001t0025g0140 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.292+5671A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562091 | ||||||
| chr3:123562104
|
G | A | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.292+5658C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562104 | ||||||
| chr3:123562161
|
A | C | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+5601T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562161 | ||||||
| chr3:123562252
|
T | C | 1 | a0002c0005t0001g0341 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.292+5510A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562252 | ||||||
| chr3:123562297
|
G | T | 2 | a0001c0003t0003g0290a0001c0003t0003g0291 | 2 | NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.292+5465C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562297 | ||||||
| chr3:123562315
|
T | G | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.292+5447A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562315 | ||||||
| chr3:123562376
|
G | A | 2 | a0001c0002t0001g0047a0001c0002t0001g0054 | 2 | HG02074.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.292+5386C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562376 | ||||||
| chr3:123562406
|
C | G | 1 | a0001c0002t0001g0034 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.292+5356G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562406 | ||||||
| chr3:123562415
|
G | C | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+5347C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562415 | ||||||
| chr3:123562517
|
ATAT | A | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+5242_292+5244d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562517 | ||||||
| chr3:123562556
|
G | C | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+5206C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562556 | ||||||
| chr3:123562623
|
T | G | 6 | a0001c0001t0004g0147a0001c0001t0004g0175a0001c0001t0004g0176others(3): Show | 6 | HG01257.hp2 HG01516.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+5139A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562623 | ||||||
| chr3:123562652
|
T | C | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+5110A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562652 | ||||||
| chr3:123562908
|
C | A | 1 | a0001c0003t0011g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292+4854G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562908 | ||||||
| chr3:123562957
|
C | T | 25 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.292+4805G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562957 | ||||||
| chr3:123563053
|
T | C | 1 | a0001c0001t0004g0179 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.292+4709A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563053 | ||||||
| chr3:123563145
|
A | C | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.292+4617T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563145 | ||||||
| chr3:123563210
|
T | A | 1 | a0001c0001t0004g0190 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.292+4552A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563210 | ||||||
| chr3:123563250
|
A | G | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+4512T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563250 | ||||||
| chr3:123563292
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.292+4470C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563292 | ||||||
| chr3:123563455
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.292+4307G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563455 | ||||||
| chr3:123563533
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.292+4229G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563533 | ||||||
| chr3:123563581
|
C | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | HG01168.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.292+4181G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563581 | ||||||
| chr3:123563638
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+4114_292+4123d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563638 | ||||||
| chr3:123563640
|
TATATACA others(3): Show |
T | 1 | a0001c0003t0012g0304 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292+4112_292+4121d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563640 | ||||||
| chr3:123563640
|
TATATACA others(5): Show |
T | 79 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0005g0113others(76): Show | 81 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.292+4110_292+4121d others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563640 | ||||||
| chr3:123563640
|
TATATACA others(7): Show |
T | 3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.292+4108_292+4121d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563640 | ||||||
| chr3:123563640
|
TATATACA others(13): Show |
T | 1 | a0001c0001t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.292+4102_292+4121d others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563640 | ||||||
| chr3:123563642
|
T | TAC | 5 | a0001c0001t0002g0182a0001c0001t0004g0004a0001c0001t0004g0109others(2): Show | 6 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+4119_292+4120i others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | ||||||
| chr3:123563642
|
TATAC | T | 6 | a0001c0001t0004g0188a0001c0002t0001g0019a0001c0002t0001g0032others(3): Show | 6 | HG03669.hp1 HG04204.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+4116_292+4119d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | ||||||
| chr3:123563642
|
TATACACA others(3): Show |
T | 5 | a0001c0003t0003g0329a0001c0003t0010g0339a0001c0003t0010g0340others(2): Show | 5 | HG02451.hp1 HG02683.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+4110_292+4119d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | ||||||
| chr3:123563642
|
TATACACA others(5): Show |
T | 31 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(28): Show | 32 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.292+4108_292+4119d others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | ||||||
| chr3:123563642
|
TATACACA others(7): Show |
T | 6 | a0001c0001t0001g0149a0001c0003t0007g0312a0001c0003t0010g0337others(3): Show | 6 | HG02055.hp1 HG02129.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+4106_292+4119d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | ||||||
| chr3:123563642
|
TATACACA others(9): Show |
T | 7 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(4): Show | 7 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+4104_292+4119d others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | ||||||
| chr3:123563644
|
T | C | 8 | a0001c0001t0002g0134a0001c0001t0002g0170a0001c0001t0002g0182others(5): Show | 9 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+4118A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | ||||||
| chr3:123563644
|
T | TAC | 20 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0146others(17): Show | 21 | HG00140.hp2 HG00544.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.292+4116_292+4117d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | ||||||
| chr3:123563644
|
T | TACAC | 7 | a0001c0001t0002g0005a0001c0001t0004g0185a0001c0001t0004g0190others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+4114_292+4117d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | ||||||
| chr3:123563644
|
T | TACACAC | 9 | a0001c0001t0004g0183a0001c0001t0004g0187a0001c0001t0004g0205others(6): Show | 9 | HG00639.hp1 HG01123.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+4112_292+4117d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | ||||||
| chr3:123563644
|
TAC | T | 29 | a0001c0001t0006g0219a0001c0001t0006g0225a0001c0001t0006g0226others(26): Show | 29 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.292+4116_292+4117d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | ||||||
| chr3:123563644
|
TACAC | T | 39 | a0001c0001t0009g0138a0001c0002t0001g0012a0001c0002t0001g0014others(36): Show | 39 | HG00423.hp2 HG01081.hp1 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.292+4114_292+4117d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | ||||||
| chr3:123563644
|
TACACAC | T | 5 | a0001c0001t0002g0124a0001c0001t0004g0179a0001c0002t0001g0034others(2): Show | 5 | HG01261.hp1 HG02015.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+4112_292+4117d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | ||||||
| chr3:123563644
|
TACACACA others(3): Show |
T | 15 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0040others(12): Show | 16 | HG00558.hp2 HG00673.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.292+4108_292+4117d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | ||||||
| chr3:123563695
|
G | A | 3 | a0001c0001t0004g0211a0001c0001t0013g0115a0001c0001t0013g0116 | 3 | HG02738.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+4067C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563695 | ||||||
| chr3:123563814
|
C | A | 1 | a0001c0003t0001g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.292+3948G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563814 | ||||||
| chr3:123563834
|
C | T | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+3928G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563834 | ||||||
| chr3:123563876
|
T | TTTAAGAA others(17): Show |
1 | a0001c0001t0002g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.292+3862_292+3885d others(26): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563876 | ||||||
| chr3:123563937
|
C | T | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+3825G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563937 | ||||||
| chr3:123563951
|
T | C | 1 | a0001c0001t0005g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.292+3811A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563951 | ||||||
| chr3:123563957
|
G | A | 162 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(159): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.292+3805C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563957 | ||||||
| chr3:123563996
|
C | T | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+3766G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563996 | ||||||
| chr3:123564067
|
G | A | 1 | a0001c0001t0015g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.292+3695C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564067 | ||||||
| chr3:123564071
|
C | G | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+3691G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564071 | ||||||
| chr3:123564073
|
T | G | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+3689A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564073 | ||||||
| chr3:123564183
|
G | A | 3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.292+3579C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564183 | ||||||
| chr3:123564217
|
C | T | 27 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0225others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+3545G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564217 | ||||||
| chr3:123564462
|
G | A | 75 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(72): Show | 76 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.292+3300C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564462 | ||||||
| chr3:123564499
|
C | G | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+3263G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564499 | ||||||
| chr3:123564503
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.292+3259C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564503 | ||||||
| chr3:123564647
|
A | C | 1 | a0001c0002t0001g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.292+3115T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564647 | ||||||
| chr3:123565089
|
C | T | 1 | a0001c0002t0001g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.292+2673G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565089 | ||||||
| chr3:123565431
|
CT | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+2330delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565431 | ||||||
| chr3:123565572
|
A | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+2190T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565572 | ||||||
| chr3:123565593
|
G | T | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+2169C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565593 | ||||||
| chr3:123565751
|
T | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+2011A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565751 | ||||||
| chr3:123565883
|
G | A | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.292+1879C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565883 | ||||||
| chr3:123566039
|
T | G | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+1723A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566039 | ||||||
| chr3:123566051
|
C | T | 87 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.292+1711G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566051 | ||||||
| chr3:123566132
|
T | C | 1 | a0001c0003t0012g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+1630A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566132 | ||||||
| chr3:123566159
|
G | A | 31 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0139others(28): Show | 31 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.292+1603C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566159 | ||||||
| chr3:123566272
|
C | T | 1 | a0001c0003t0003g0297 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.292+1490G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566272 | ||||||
| chr3:123566450
|
C | T | 1 | a0001c0002t0001g0029 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.292+1312G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566450 | ||||||
| chr3:123566503
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+1259G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566503 | ||||||
| chr3:123566630
|
TG | T | 341 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(338): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.292+1131delC | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566630 | ||||||
| chr3:123566727
|
T | C | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+1035A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566727 | ||||||
| chr3:123566853
|
A | G | 3 | a0001c0001t0004g0164a0001c0001t0004g0184a0001c0001t0004g0185 | 3 | NA18949.hp2 NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.292+909T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566853 | ||||||
| chr3:123566895
|
A | G | 1 | a0001c0001t0002g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.292+867T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566895 | ||||||
| chr3:123567009
|
C | T | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+753G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567009 | ||||||
| chr3:123567254
|
T | G | 162 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(159): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.292+508A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567254 | ||||||
| chr3:123567312
|
C | T | 1 | a0001c0001t0006g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+450G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567312 | ||||||
| chr3:123567346
|
A | G | 1 | a0001c0001t0004g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.292+416T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567346 | ||||||
| chr3:123567369
|
A | G | 75 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0001t0006g0218others(72): Show | 77 | HG00544.hp2 HG01109.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.292+393T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567369 | ||||||
| chr3:123567946
|
C | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-166G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123567946 | ||||||
| chr3:123567951
|
T | C | 1 | a0001c0003t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.274-171A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123567951 | ||||||
| chr3:123567966
|
A | G | 7 | a0001c0002t0008g0013a0001c0002t0008g0065a0001c0002t0008g0070others(4): Show | 7 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-186T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123567966 | ||||||
| chr3:123568105
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-325T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568105 | ||||||
| chr3:123568128
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.274-348T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568128 | ||||||
| chr3:123568152
|
C | T | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-372G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568152 | ||||||
| chr3:123568194
|
T | C | 1 | a0001c0003t0003g0289 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274-414A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568194 | ||||||
| chr3:123568197
|
C | A | 1 | a0001c0001t0002g0135 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274-417G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568197 | ||||||
| chr3:123568372
|
C | T | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-592G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568372 | ||||||
| chr3:123568424
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.274-644C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568424 | ||||||
| chr3:123568519
|
C | T | 135 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.274-739G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568519 | ||||||
| chr3:123568618
|
C | G | 2 | a0001c0001t0002g0201a0001c0001t0002g0213 | 2 | HG02145.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.274-838G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568618 | ||||||
| chr3:123568618
|
C | T | 1 | a0001c0002t0002g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.274-838G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568618 | ||||||
| chr3:123568713
|
T | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.274-933A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568713 | ||||||
| chr3:123568865
|
C | G | 1 | a0001c0003t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.274-1085G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568865 | ||||||
| chr3:123568959
|
T | C | 38 | a0001c0001t0002g0182a0001c0001t0004g0004a0001c0001t0004g0109others(35): Show | 40 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.274-1179A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568959 | ||||||
| chr3:123568970
|
T | G | 4 | a0001c0001t0002g0197a0001c0003t0005g0300a0001c0003t0005g0301others(1): Show | 4 | HG02258.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-1190A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568970 | ||||||
| chr3:123569046
|
A | G | 48 | a0001c0001t0003g0112a0001c0001t0003g0154a0001c0003t0003g0006others(45): Show | 50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.274-1266T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569046 | ||||||
| chr3:123569103
|
G | A | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-1323C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569103 | ||||||
| chr3:123569165
|
C | G | 2 | a0001c0001t0006g0226a0001c0001t0006g0232 | 2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.274-1385G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569165 | ||||||
| chr3:123569305
|
G | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.274-1525C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569305 | ||||||
| chr3:123569491
|
A | AGCTGGGA others(15): Show |
1 | a0001c0001t0006g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274-1733_274-1712d others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569491 | ||||||
| chr3:123569512
|
C | T | 1 | a0001c0003t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.274-1732G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569512 | ||||||
| chr3:123569605
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.274-1825C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569605 | ||||||
| chr3:123569699
|
C | A | 106 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251others(103): Show | 107 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.274-1919G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569699 | ||||||
| chr3:123569725
|
C | T | 2 | a0001c0001t0004g0109a0001c0001t0004g0110 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.274-1945G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569725 | ||||||
| chr3:123569748
|
G | A | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.274-1968C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569748 | ||||||
| chr3:123569813
|
C | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.274-2033G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569813 | ||||||
| chr3:123569850
|
A | G | 3 | a0001c0002t0005g0068a0001c0002t0005g0069a0001c0002t0005g0073 | 3 | HG02970.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.274-2070T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569850 | ||||||
| chr3:123569888
|
C | T | 6 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-2108G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569888 | ||||||
| chr3:123569942
|
T | C | 1 | a0001c0003t0003g0276 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.274-2162A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569942 | ||||||
| chr3:123569988
|
C | CA | 6 | a0001c0001t0002g0165a0001c0001t0002g0197a0001c0001t0004g0188others(3): Show | 6 | HG02080.hp1 HG03239.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-2209dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CA | C | 18 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0167others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.274-2209delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAA | C | 9 | a0001c0001t0002g0005a0001c0001t0002g0108a0001c0001t0002g0166others(6): Show | 11 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-2210_274-2209d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAA | C | 6 | a0001c0001t0002g0155a0001c0001t0002g0196a0001c0002t0005g0097others(3): Show | 6 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-2211_274-2209d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAA | C | 9 | a0001c0001t0002g0169a0001c0001t0005g0113a0001c0001t0005g0114others(6): Show | 9 | HG00544.hp1 HG01358.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-2212_274-2209d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAA | C | 13 | a0001c0001t0002g0120a0001c0001t0002g0168a0001c0001t0005g0199others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.274-2213_274-2209d others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAA | C | 7 | a0001c0001t0005g0173a0001c0002t0005g0064a0001c0002t0005g0066others(4): Show | 7 | HG00639.hp2 HG00673.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-2214_274-2209d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0003g0154a0001c0001t0013g0115a0001c0001t0013g0116others(11): Show | 14 | HG00673.hp1 HG02083.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-2217_274-2209d others(11): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(3): Show |
C | 44 | a0001c0001t0003g0112a0001c0001t0015g0223a0001c0002t0001g0034others(41): Show | 46 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.274-2218_274-2209d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0003t0001g0008a0001c0003t0003g0269a0001c0003t0003g0293others(2): Show | 6 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-2219_274-2209d others(13): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(5): Show |
C | 20 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(17): Show | 20 | HG00738.hp1 HG01071.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.274-2220_274-2209d others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(6): Show |
C | 27 | a0001c0001t0001g0148a0001c0001t0002g0220a0001c0001t0002g0251others(24): Show | 27 | HG00323.hp2 HG00735.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.274-2221_274-2209d others(15): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(7): Show |
C | 86 | a0001c0001t0006g0219a0001c0001t0006g0225a0001c0001t0006g0228others(83): Show | 87 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.274-2222_274-2209d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0006g0226a0001c0001t0006g0227a0001c0001t0006g0237others(2): Show | 5 | HG01167.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-2223_274-2209d others(17): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0002g0191a0001c0002t0004g0099 | 2 | HG01433.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.274-2224_274-2209d others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0002g0198a0001c0002t0005g0020 | 2 | HG02280.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.274-2225_274-2209d others(19): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(11): Show |
C | 6 | a0001c0001t0004g0147a0001c0001t0004g0175a0001c0001t0004g0176others(3): Show | 6 | HG01516.hp1 HG02602.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-2226_274-2209d others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0002g0137a0001c0001t0004g0190a0001c0002t0001g0029 | 3 | HG01257.hp2 HG02027.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.274-2227_274-2209d others(21): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123569988
|
CAAAAAAA others(13): Show |
C | 35 | a0001c0001t0002g0003a0001c0001t0002g0117a0001c0001t0002g0118others(32): Show | 36 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.274-2228_274-2209d others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | ||||||
| chr3:123570079
|
A | G | 5 | a0001c0002t0005g0094a0001c0003t0010g0337a0001c0003t0010g0338others(2): Show | 5 | HG01433.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-2299T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570079 | ||||||
| chr3:123570264
|
T | C | 9 | a0001c0001t0031g0342a0001c0003t0007g0305a0001c0003t0007g0306others(6): Show | 9 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-2484A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570264 | ||||||
| chr3:123570504
|
A | C | 23 | a0001c0001t0003g0112a0001c0003t0003g0253a0001c0003t0003g0254others(20): Show | 23 | HG00544.hp2 HG01928.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.274-2724T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570504 | ||||||
| chr3:123570656
|
C | T | 1 | a0001c0003t0003g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.274-2876G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570656 | ||||||
| chr3:123570724
|
C | T | 1 | a0001c0001t0019g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.274-2944G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570724 | ||||||
| chr3:123570748
|
C | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.274-2968G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570748 | ||||||
| chr3:123570832
|
T | G | 226 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(223): Show | 230 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.274-3052A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570832 | ||||||
| chr3:123570867
|
G | A | 5 | a0001c0003t0003g0286a0001c0003t0003g0287a0001c0003t0003g0288others(2): Show | 5 | HG02071.hp1 NA18945.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3087C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570867 | ||||||
| chr3:123570917
|
T | TAC | 44 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(41): Show | 45 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.274-3139_274-3138d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACAC | 6 | a0001c0001t0002g0195a0001c0001t0006g0250a0001c0001t0015g0223others(3): Show | 6 | HG00639.hp2 HG01167.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-3141_274-3138d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(1): Show |
30 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0199others(27): Show | 31 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.274-3145_274-3138d others(10): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(3): Show |
15 | a0001c0001t0005g0173a0001c0002t0001g0011a0001c0002t0001g0024others(12): Show | 15 | HG00597.hp2 HG02132.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.274-3147_274-3138d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(5): Show |
24 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0030others(21): Show | 24 | HG00423.hp2 HG01884.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.274-3149_274-3138d others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(7): Show |
35 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0012others(32): Show | 36 | HG00558.hp2 HG00673.hp1 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.274-3151_274-3138d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(9): Show |
22 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0002t0001g0010others(19): Show | 23 | HG00140.hp1 HG00323.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.274-3153_274-3138d others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(11): Show |
12 | a0001c0001t0003g0112a0001c0002t0001g0059a0001c0002t0001g0060others(9): Show | 12 | HG00639.hp1 HG01255.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-3155_274-3138d others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(13): Show |
21 | a0001c0002t0001g0090a0001c0003t0003g0254a0001c0003t0003g0255others(18): Show | 21 | HG00544.hp2 HG01109.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.274-3157_274-3138d others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(15): Show |
15 | a0001c0001t0030g0252a0001c0003t0003g0007a0001c0003t0003g0253others(12): Show | 16 | HG01943.hp1 HG02071.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.274-3159_274-3138d others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(17): Show |
2 | a0001c0003t0003g0290a0001c0003t0003g0291 | 2 | NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.274-3161_274-3138d others(26): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(19): Show |
1 | a0001c0003t0003g0292 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.274-3163_274-3138d others(28): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570917
|
T | TACACACA others(21): Show |
1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.274-3138_274-3137i others(30): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | ||||||
| chr3:123570943
|
C | CACACACA others(17): Show |
1 | a0001c0001t0002g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.274-3164_274-3163i others(26): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570943 | ||||||
| chr3:123570943
|
C | CACACACA others(13): Show |
1 | a0001c0001t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.274-3164_274-3163i others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570943 | ||||||
| chr3:123570945
|
T | C | 2 | a0001c0001t0002g0221a0001c0001t0002g0251 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.274-3165A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570945 | ||||||
| chr3:123571054
|
G | A | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251 | 3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.274-3274C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571054 | ||||||
| chr3:123571124
|
T | C | 6 | a0001c0002t0001g0101a0001c0002t0004g0002a0001c0002t0004g0099others(3): Show | 7 | NA18946.hp2 NA18964.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-3344A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571124 | ||||||
| chr3:123571259
|
G | A | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-3479C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571259 | ||||||
| chr3:123571376
|
A | G | 72 | a0001c0001t0003g0112a0001c0003t0001g0008a0001c0003t0001g0314others(69): Show | 75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.274-3596T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571376 | ||||||
| chr3:123571420
|
C | A | 2 | a0001c0001t0015g0223a0001c0001t0015g0224 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.274-3640G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571420 | ||||||
| chr3:123571470
|
C | G | 4 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-3690G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571470 | ||||||
| chr3:123571526
|
G | A | 108 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(105): Show | 109 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.274-3746C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571526 | ||||||
| chr3:123571568
|
C | T | 32 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.274-3788G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571568 | ||||||
| chr3:123571609
|
G | A | 1 | a0001c0003t0003g0293 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.274-3829C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571609 | ||||||
| chr3:123571774
|
G | A | 1 | a0001c0002t0001g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.274-3994C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571774 | ||||||
| chr3:123571821
|
A | G | 33 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(30): Show | 33 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.274-4041T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571821 | ||||||
| chr3:123572244
|
A | G | 231 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(228): Show | 235 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.274-4464T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572244 | ||||||
| chr3:123572260
|
C | T | 103 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(100): Show | 104 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.274-4480G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572260 | ||||||
| chr3:123572316
|
C | T | 108 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(105): Show | 109 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.274-4536G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572316 | ||||||
| chr3:123572511
|
G | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-4731C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572511 | ||||||
| chr3:123572619
|
T | A | 231 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(228): Show | 235 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.274-4839A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572619 | ||||||
| chr3:123572649
|
C | T | 18 | a0001c0001t0002g0117a0001c0001t0002g0123a0001c0001t0002g0124others(15): Show | 18 | HG00423.hp1 HG00558.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.274-4869G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572649 | ||||||
| chr3:123572662
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.274-4882A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572662 | ||||||
| chr3:123572713
|
GTTCAAT | G | 45 | a0001c0001t0003g0112a0001c0003t0003g0006a0001c0003t0003g0007others(42): Show | 47 | HG00544.hp2 HG01928.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.274-4939_274-4934d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572713 | ||||||
| chr3:123572772
|
G | C | 192 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.274-4992C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572772 | ||||||
| chr3:123572861
|
C | T | 3 | a0001c0001t0006g0234a0001c0001t0006g0235a0001c0001t0006g0236 | 3 | HG02976.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.274-5081G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572861 | ||||||
| chr3:123572940
|
G | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.274-5160C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572940 | ||||||
| chr3:123573081
|
A | C | 1 | a0001c0001t0006g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.274-5301T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573081 | ||||||
| chr3:123573184
|
T | G | 25 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0173others(22): Show | 25 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.274-5404A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573184 | ||||||
| chr3:123573212
|
T | C | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-5432A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573212 | ||||||
| chr3:123573222
|
G | A | 33 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0173others(30): Show | 33 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-5442C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573222 | ||||||
| chr3:123573337
|
C | T | 1 | a0001c0001t0006g0225 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.274-5557G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573337 | ||||||
| chr3:123573439
|
G | A | 1 | a0001c0002t0001g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.274-5659C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573439 | ||||||
| chr3:123573636
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.274-5856A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573636 | ||||||
| chr3:123573737
|
G | A | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-5957C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573737 | ||||||
| chr3:123573737
|
G | C | 1 | a0001c0003t0003g0294 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.274-5957C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573737 | ||||||
| chr3:123573920
|
G | C | 5 | a0001c0002t0005g0094a0001c0002t0005g0095a0001c0002t0005g0096others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-6140C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573920 | ||||||
| chr3:123573941
|
G | A | 10 | a0001c0003t0003g0313a0001c0003t0003g0327a0001c0003t0003g0329others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-6161C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573941 | ||||||
| chr3:123574036
|
A | G | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-6256T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574036 | ||||||
| chr3:123574160
|
A | C | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.274-6380T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574160 | ||||||
| chr3:123574257
|
G | A | 103 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(100): Show | 104 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.274-6477C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574257 | ||||||
| chr3:123574444
|
T | C | 231 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(228): Show | 235 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.274-6664A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574444 | ||||||
| chr3:123574459
|
T | C | 3 | a0001c0001t0002g0120a0001c0001t0002g0168a0001c0001t0002g0169 | 3 | HG00544.hp1 NA18942.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.274-6679A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574459 | ||||||
| chr3:123574637
|
G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274-6857C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574637 | ||||||
| chr3:123574680
|
CAT | C | 11 | a0001c0003t0001g0008a0001c0003t0001g0314a0001c0003t0001g0315others(8): Show | 12 | HG00140.hp1 HG00323.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-6902_274-6901d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574680 | ||||||
| chr3:123574742
|
C | T | 109 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(106): Show | 110 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.274-6962G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574742 | ||||||
| chr3:123574754
|
A | T | 1 | a0001c0003t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.274-6974T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574754 | ||||||
| chr3:123575011
|
T | C | 1 | a0001c0001t0004g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.273+7201A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575011 | ||||||
| chr3:123575068
|
A | G | 1 | a0001c0002t0001g0022 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.273+7144T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575068 | ||||||
| chr3:123575110
|
AT | A | 125 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(122): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.273+7101delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575110 | ||||||
| chr3:123575384
|
T | C | 1 | a0001c0001t0027g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.273+6828A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575384 | ||||||
| chr3:123575506
|
C | G | 5 | a0001c0002t0005g0094a0001c0002t0005g0095a0001c0002t0005g0096others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+6706G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575506 | ||||||
| chr3:123575622
|
T | C | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+6590A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575622 | ||||||
| chr3:123575689
|
T | G | 186 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(183): Show | 190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+6523A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575689 | ||||||
| chr3:123575739
|
C | T | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+6473G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575739 | ||||||
| chr3:123575917
|
G | A | 14 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0080others(11): Show | 14 | NA18959.hp1 NA18962.hp1 NA18964.hp1 others(11): Show |
intron_variant | MODIFIER | c.273+6295C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575917 | ||||||
| chr3:123575938
|
T | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+6274A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575938 | ||||||
| chr3:123576059
|
T | C | 1 | a0001c0003t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273+6153A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576059 | ||||||
| chr3:123576186
|
T | A | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+6026A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576186 | ||||||
| chr3:123576249
|
CT | C | 225 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(222): Show | 229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+5962delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576249 | ||||||
| chr3:123576266
|
T | C | 1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.273+5946A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576266 | ||||||
| chr3:123576726
|
C | T | 1 | a0001c0002t0001g0016 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.273+5486G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576726 | ||||||
| chr3:123576849
|
A | C | 2 | a0001c0001t0015g0223a0001c0001t0015g0224 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.273+5363T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576849 | ||||||
| chr3:123576970
|
A | C | 1 | a0001c0001t0027g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.273+5242T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576970 | ||||||
| chr3:123576974
|
C | G | 225 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(222): Show | 229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+5238G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576974 | ||||||
| chr3:123577040
|
T | TCAATTCC others(19): Show |
1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+5146_273+5171d others(28): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577040 | ||||||
| chr3:123577094
|
A | G | 72 | a0001c0003t0001g0008a0001c0003t0001g0314a0001c0003t0001g0315others(69): Show | 75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.273+5118T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577094 | ||||||
| chr3:123577105
|
C | T | 186 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(183): Show | 190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+5107G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577105 | ||||||
| chr3:123577211
|
T | C | 1 | a0001c0001t0004g0190 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.273+5001A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577211 | ||||||
| chr3:123577326
|
T | C | 176 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(173): Show | 180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.273+4886A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577326 | ||||||
| chr3:123577396
|
C | T | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+4816G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577396 | ||||||
| chr3:123577424
|
A | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.273+4788T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577424 | ||||||
| chr3:123577437
|
T | C | 225 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(222): Show | 229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+4775A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577437 | ||||||
| chr3:123577471
|
A | G | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.273+4741T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577471 | ||||||
| chr3:123577481
|
T | C | 225 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(222): Show | 229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+4731A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577481 | ||||||
| chr3:123577620
|
C | CA | 35 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(32): Show | 35 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.273+4591dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577620 | ||||||
| chr3:123577620
|
CA | C | 172 | a0001c0001t0002g0120a0001c0001t0013g0115a0001c0001t0013g0116others(169): Show | 176 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.273+4591delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577620 | ||||||
| chr3:123577620
|
CAA | C | 7 | a0001c0002t0001g0019a0001c0002t0005g0020a0001c0002t0005g0021others(4): Show | 7 | HG01516.hp2 NA18957.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+4590_273+4591d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577620 | ||||||
| chr3:123577629
|
A | C | 8 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.273+4583T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577629 | ||||||
| chr3:123577846
|
A | G | 225 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(222): Show | 229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+4366T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577846 | ||||||
| chr3:123577896
|
C | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.273+4316G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577896 | ||||||
| chr3:123577927
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273+4285G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577927 | ||||||
| chr3:123577930
|
G | C | 176 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(173): Show | 180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.273+4282C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577930 | ||||||
| chr3:123578028
|
ACCCCACT others(4): Show |
A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4173_273+4183d others(13): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578028 | ||||||
| chr3:123578038
|
C | G | 3 | a0001c0003t0005g0300a0001c0003t0005g0301a0001c0003t0005g0302 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.273+4174G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578038 | ||||||
| chr3:123578052
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4160G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578052 | ||||||
| chr3:123578059
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4153T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578059 | ||||||
| chr3:123578060
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4152A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578060 | ||||||
| chr3:123578061
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4151A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578061 | ||||||
| chr3:123578063
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4149G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578063 | ||||||
| chr3:123578064
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4148A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578064 | ||||||
| chr3:123578066
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4146A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578066 | ||||||
| chr3:123578067
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4145T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578067 | ||||||
| chr3:123578076
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4136G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578076 | ||||||
| chr3:123578106
|
TTATAAAT others(4): Show |
T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4095_273+4105d others(13): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578106 | ||||||
| chr3:123578118
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4094A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578118 | ||||||
| chr3:123578120
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4092T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578120 | ||||||
| chr3:123578121
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4091A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578121 | ||||||
| chr3:123578143
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4069G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578143 | ||||||
| chr3:123578147
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4065G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578147 | ||||||
| chr3:123578148
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4064A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578148 | ||||||
| chr3:123578150
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4062G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578150 | ||||||
| chr3:123578151
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4061A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578151 | ||||||
| chr3:123578152
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4060A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578152 | ||||||
| chr3:123578156
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4056G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578156 | ||||||
| chr3:123578170
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4042T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578170 | ||||||
| chr3:123578171
|
G | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4041C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578171 | ||||||
| chr3:123578175
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4037A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578175 | ||||||
| chr3:123578176
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4036T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578176 | ||||||
| chr3:123578196
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4016A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578196 | ||||||
| chr3:123578209
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4003T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578209 | ||||||
| chr3:123578214
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3998A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578214 | ||||||
| chr3:123578221
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3991T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578221 | ||||||
| chr3:123578232
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3980G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578232 | ||||||
| chr3:123578233
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3979G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578233 | ||||||
| chr3:123578234
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3978T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578234 | ||||||
| chr3:123578235
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3977A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578235 | ||||||
| chr3:123578239
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3973G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578239 | ||||||
| chr3:123578257
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3955A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578257 | ||||||
| chr3:123578262
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3950A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578262 | ||||||
| chr3:123578271
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3941A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578271 | ||||||
| chr3:123578273
|
G | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3939C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578273 | ||||||
| chr3:123578275
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3937A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578275 | ||||||
| chr3:123578277
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3935G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578277 | ||||||
| chr3:123578279
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3933A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578279 | ||||||
| chr3:123578280
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3932A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578280 | ||||||
| chr3:123578281
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3931A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578281 | ||||||
| chr3:123578290
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3922T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578290 | ||||||
| chr3:123578299
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3913G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578299 | ||||||
| chr3:123578302
|
G | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3910C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578302 | ||||||
| chr3:123578303
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3909G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578303 | ||||||
| chr3:123578305
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3907G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578305 | ||||||
| chr3:123578306
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3906A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578306 | ||||||
| chr3:123578312
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3900G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578312 | ||||||
| chr3:123578321
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3891T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578321 | ||||||
| chr3:123578323
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3889A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578323 | ||||||
| chr3:123578324
|
G | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3888C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578324 | ||||||
| chr3:123578326
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3886T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578326 | ||||||
| chr3:123578332
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3880T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578332 | ||||||
| chr3:123578339
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3873A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578339 | ||||||
| chr3:123578342
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3870G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578342 | ||||||
| chr3:123578343
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3869A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578343 | ||||||
| chr3:123578344
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3868G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578344 | ||||||
| chr3:123578345
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3867T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578345 | ||||||
| chr3:123578353
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3859G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578353 | ||||||
| chr3:123578354
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3858A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578354 | ||||||
| chr3:123578361
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3851G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578361 | ||||||
| chr3:123578376
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3836A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578376 | ||||||
| chr3:123578377
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3835G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578377 | ||||||
| chr3:123578378
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3834G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578378 | ||||||
| chr3:123578379
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3833A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578379 | ||||||
| chr3:123578384
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3828G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578384 | ||||||
| chr3:123578387
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3825G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578387 | ||||||
| chr3:123578394
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3818G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578394 | ||||||
| chr3:123578415
|
C | T | 4 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0251others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+3797G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578415 | ||||||
| chr3:123578559
|
T | C | 100 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(97): Show | 101 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.273+3653A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578559 | ||||||
| chr3:123578589
|
T | C | 223 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(220): Show | 227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.273+3623A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578589 | ||||||
| chr3:123578664
|
T | C | 186 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(183): Show | 190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+3548A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578664 | ||||||
| chr3:123578893
|
G | C | 176 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(173): Show | 180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.273+3319C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578893 | ||||||
| chr3:123579093
|
T | C | 2 | a0001c0003t0012g0303a0001c0003t0012g0304 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+3119A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579093 | ||||||
| chr3:123579211
|
G | A | 1 | a0001c0001t0004g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.273+3001C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579211 | ||||||
| chr3:123579299
|
G | GT | 13 | a0001c0001t0002g0005a0001c0001t0002g0171a0001c0001t0002g0172others(10): Show | 14 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+2912dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579299 | ||||||
| chr3:123579369
|
G | A | 95 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(92): Show | 96 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.273+2843C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579369 | ||||||
| chr3:123579450
|
C | T | 1 | a0001c0003t0003g0254 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.273+2762G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579450 | ||||||
| chr3:123579474
|
A | T | 1 | a0001c0002t0001g0016 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.273+2738T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579474 | ||||||
| chr3:123579523
|
C | T | 37 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(34): Show | 37 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.273+2689G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579523 | ||||||
| chr3:123579586
|
T | C | 1 | a0001c0002t0005g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.273+2626A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579586 | ||||||
| chr3:123579768
|
T | C | 186 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(183): Show | 190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+2444A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579768 | ||||||
| chr3:123579772
|
G | A | 1 | a0001c0003t0001g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.273+2440C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579772 | ||||||
| chr3:123579824
|
G | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+2388C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579824 | ||||||
| chr3:123579887
|
G | A | 1 | a0001c0003t0003g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.273+2325C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579887 | ||||||
| chr3:123579999
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0171a0001c0001t0002g0172others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+2213A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579999 | ||||||
| chr3:123580166
|
C | CA | 48 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(45): Show | 49 | HG00140.hp1 HG01167.hp1 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.273+2045dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580166 | ||||||
| chr3:123580174
|
A | G | 98 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(95): Show | 99 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.273+2038T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580174 | ||||||
| chr3:123580275
|
A | G | 186 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(183): Show | 190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+1937T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580275 | ||||||
| chr3:123580358
|
C | T | 1 | a0001c0003t0005g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.273+1854G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580358 | ||||||
| chr3:123580389
|
T | C | 32 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.273+1823A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580389 | ||||||
| chr3:123580620
|
T | C | 1 | a0001c0001t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.273+1592A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580620 | ||||||
| chr3:123580733
|
C | T | 176 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(173): Show | 180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.273+1479G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580733 | ||||||
| chr3:123580791
|
GA | G | 98 | a0001c0001t0002g0117a0001c0002t0001g0001a0001c0002t0001g0009others(95): Show | 99 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.273+1420delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580791 | ||||||
| chr3:123580853
|
AT | A | 244 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(241): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.273+1358delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580853 | ||||||
| chr3:123580853
|
ATT | A | 15 | a0001c0001t0002g0251a0001c0002t0001g0093a0001c0003t0007g0306others(12): Show | 15 | HG00099.hp1 HG00642.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.273+1357_273+1358d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580853 | ||||||
| chr3:123580878
|
CAG | C | 5 | a0001c0002t0005g0094a0001c0002t0005g0095a0001c0002t0005g0096others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+1332_273+1333d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580878 | ||||||
| chr3:123580916
|
C | T | 2 | a0001c0001t0013g0115a0001c0001t0013g0116 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.273+1296G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580916 | ||||||
| chr3:123581010
|
C | T | 2 | a0001c0001t0005g0113a0001c0001t0005g0114 | 2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.273+1202G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581010 | ||||||
| chr3:123581035
|
C | T | 2 | a0001c0001t0006g0218a0001c0001t0019g0217 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.273+1177G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581035 | ||||||
| chr3:123581118
|
C | T | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+1094G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581118 | ||||||
| chr3:123581119
|
G | A | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+1093C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581119 | ||||||
| chr3:123581363
|
A | G | 1 | a0001c0001t0003g0112 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.273+849T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581363 | ||||||
| chr3:123581451
|
T | C | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+761A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581451 | ||||||
| chr3:123581501
|
T | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.273+711A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581501 | ||||||
| chr3:123581657
|
T | C | 1 | a0001c0003t0001g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.273+555A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581657 | ||||||
| chr3:123581839
|
C | G | 7 | a0001c0003t0001g0008a0001c0003t0001g0314a0001c0003t0001g0315others(4): Show | 8 | HG00140.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+373G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581839 | ||||||
| chr3:123581878
|
C | A | 9 | a0001c0003t0003g0313a0001c0003t0003g0329a0001c0003t0003g0330others(6): Show | 9 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+334G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581878 | ||||||
| chr3:123581940
|
T | C | 37 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(34): Show | 37 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.273+272A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581940 | ||||||
| chr3:123582009
|
A | G | 1 | a0001c0002t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.273+203T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123582009 | ||||||
| chr3:123582159
|
G | C | 1 | a0001c0003t0003g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.273+53C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123582159 | ||||||
| chr3:123582177
|
G | A | 10 | a0001c0003t0007g0305a0001c0003t0007g0306a0001c0003t0007g0307others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+35C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123582177 | ||||||
| chr3:123582395
|
C | G | 223 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(220): Show | 227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.156-66G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582395 | ||||||
| chr3:123582537
|
G | A | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156-208C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582537 | ||||||
| chr3:123582589
|
C | G | 3 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0111 | 3 | HG01168.hp1 HG01169.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.156-260G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582589 | ||||||
| chr3:123582654
|
G | A | 1 | a0001c0003t0003g0296 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.156-325C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582654 | ||||||
| chr3:123582671
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.156-342G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582671 | ||||||
| chr3:123582692
|
A | G | 1 | a0001c0002t0001g0009 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.156-363T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582692 | ||||||
| chr3:123582791
|
T | C | 25 | a0001c0003t0001g0008a0001c0003t0001g0314a0001c0003t0001g0315others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.156-462A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582791 | ||||||
| chr3:123582839
|
T | C | 1 | a0001c0001t0002g0201 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.156-510A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582839 | ||||||
| chr3:123583083
|
G | A | 11 | a0001c0001t0004g0202a0001c0001t0004g0203a0001c0001t0004g0204others(8): Show | 11 | HG00099.hp2 HG01123.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.156-754C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583083 | ||||||
| chr3:123583109
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.156-780A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583109 | ||||||
| chr3:123583202
|
TA | T | 72 | a0001c0003t0001g0008a0001c0003t0001g0314a0001c0003t0001g0315others(69): Show | 75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.156-874delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583202 | ||||||
| chr3:123583430
|
G | GT | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-1102dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583430 | ||||||
| chr3:123583437
|
T | A | 2 | a0001c0001t0031g0342a0001c0002t0001g0105 | 2 | HG01515.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.156-1108A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583437 | ||||||
| chr3:123583688
|
T | C | 37 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(34): Show | 37 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.155+1185A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583688 | ||||||
| chr3:123583847
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.155+1026C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583847 | ||||||
| chr3:123584146
|
T | C | 1 | a0001c0003t0003g0297 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.155+727A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584146 | ||||||
| chr3:123584245
|
A | T | 1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.155+628T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584245 | ||||||
| chr3:123584440
|
C | T | 2 | a0001c0003t0014g0298a0001c0003t0014g0299 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.155+433G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584440 | ||||||
| chr3:123584457
|
ACT | A | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG00597.hp1 HG02155.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.155+414_155+415del others(2): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584457 | ||||||
| chr3:123584476
|
T | C | 25 | a0001c0003t0001g0008a0001c0003t0001g0314a0001c0003t0001g0315others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.155+397A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584476 | ||||||
| chr3:123584508
|
G | A | 1 | a0001c0002t0001g0106 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.155+365C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584508 | ||||||
| chr3:123584639
|
C | A | 37 | a0001c0001t0001g0222a0001c0001t0001g0246a0001c0001t0001g0247others(34): Show | 37 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.155+234G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584639 | ||||||
| chr3:123584650
|
G | A | 47 | a0001c0003t0003g0006a0001c0003t0003g0007a0001c0003t0003g0253others(44): Show | 49 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(46): Show |
intron_variant | MODIFIER | c.155+223C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584650 | ||||||
| chr3:123584744
|
T | G | 4 | a0001c0003t0010g0337a0001c0003t0010g0338a0001c0003t0010g0339others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+129A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584744 | ||||||
| chr3:123584806
|
C | T | 47 | a0001c0003t0003g0006a0001c0003t0003g0007a0001c0003t0003g0253others(44): Show | 49 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(46): Show |
intron_variant | MODIFIER | c.155+67G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584806 |