Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 65985 |
|---|---|
| ensemblid | ENSG00000081760.17 |
| hgncid | 21298 |
| symbol | AACS |
| name | acetoacetyl-CoA synthetase |
| refseq_nuc | NM_023928.5 |
| refseq_prot | NP_076417.2 |
| ensembl_nuc | ENST00000316519.11 |
| ensembl_prot | ENSP00000324842.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 125065435 |
| end | 125143316 |
| strand | + |
| ver | v1.2 |
| region | chr12:125065435-125143316 |
| region5000 | chr12:125060435-125148316 |
| regionname0 | AACS_chr12_125065435_125143316 |
| regionname5000 | AACS_chr12_125060435_125148316 |
| 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 | 1/0 | 672 | 273 | 54 | 58 | 120 | 12 | 28 | 91 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002 | 0/1 | 672 | 83 | 33 | 10 | 24 | 2 | 13 | 23 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0003 | 0/0 | 672 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0004 | 0/0 | 672 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0005 | 0/0 | 672 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0006 | 0/0 | 672 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0007 | 0/0 | 672 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0008 | 0/0 | 672 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0009 | 0/0 | 672 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0010 | 0/0 | 672 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2019 | 226 | 45 | 58 | 84 | 12 | 26 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0002 | 0/1 | 2019 | 63 | 19 | 9 | 19 | 2 | 13 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0003 | 0/0 | 2019 | 23 | 4 | 0 | 17 | 0 | 2 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0004 | 0/0 | 2019 | 16 | 2 | 0 | 14 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0005 | 0/0 | 2019 | 8 | 8 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0006 | 0/0 | 2019 | 4 | 0 | 0 | 4 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0007 | 0/0 | 2019 | 3 | 3 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0008 | 0/0 | 2019 | 2 | 0 | 0 | 2 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0009 | 0/0 | 2019 | 2 | 2 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0010 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0011 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0012 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0013 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0014 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0015 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0016 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0017 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0018 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0019 | 0/0 | 2019 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0020 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0021 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0022 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0023 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0024 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0025 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| c0026 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| 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 | 1/0 | 1238 | 216 | 81 | 36 | 67 | 4 | 27 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0002 | 0/0 | 1238 | 74 | 1 | 13 | 49 | 4 | 7 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0003 | 0/0 | 1238 | 24 | 0 | 11 | 13 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0004 | 0/0 | 1238 | 16 | 0 | 0 | 15 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0005 | 0/0 | 1238 | 14 | 8 | 4 | 0 | 2 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0006 | 0/1 | 1238 | 12 | 0 | 5 | 0 | 4 | 2 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0007 | 0/0 | 1238 | 4 | 0 | 0 | 0 | 0 | 4 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0008 | 0/0 | 1238 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0009 | 0/0 | 1238 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0010 | 0/0 | 1238 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| t0011 | 0/0 | 1238 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| 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 | 0 | 0 | 2 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2019 | 226 | 45 | 58 | 84 | 12 | 26 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0003 | 0/0 | 2019 | 23 | 4 | 0 | 17 | 0 | 2 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0004 | 0/0 | 2019 | 16 | 2 | 0 | 14 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0008 | 0/0 | 2019 | 2 | 0 | 0 | 2 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0009 | 0/0 | 2019 | 2 | 2 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0012 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0015 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0017 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0020 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0002 | 0/1 | 2019 | 63 | 19 | 9 | 19 | 2 | 13 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0005 | 0/0 | 2019 | 8 | 8 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0006 | 0/0 | 2019 | 4 | 0 | 0 | 4 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0007 | 0/0 | 2019 | 3 | 3 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0010 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0011 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0021 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0025 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0026 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0003c0019 | 0/0 | 2019 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0004c0018 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0005c0014 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0006c0013 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0007c0016 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0008c0023 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0009c0024 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0010c0022 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3256 | 109 | 37 | 24 | 28 | 2 | 17 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0001t0002 | 0/0 | 3256 | 69 | 1 | 13 | 45 | 4 | 6 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0001t0003 | 0/0 | 3256 | 21 | 0 | 11 | 10 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0001t0005 | 0/0 | 3256 | 13 | 7 | 4 | 0 | 2 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0001t0006 | 0/0 | 3256 | 11 | 0 | 5 | 0 | 4 | 2 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0001t0008 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0001t0010 | 0/0 | 3256 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0001t0011 | 0/0 | 3256 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0003t0001 | 0/0 | 3256 | 21 | 4 | 0 | 16 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0003t0004 | 0/0 | 3256 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0003t0009 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0004t0001 | 0/0 | 3256 | 2 | 2 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0004t0004 | 0/0 | 3256 | 14 | 0 | 0 | 14 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0008t0001 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0008t0002 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0009t0001 | 0/0 | 3256 | 2 | 2 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0012t0004 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0015t0001 | 0/0 | 3256 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0017t0002 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0001c0020t0002 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0002t0001 | 0/0 | 3256 | 54 | 18 | 9 | 17 | 2 | 8 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0002t0002 | 0/0 | 3256 | 2 | 0 | 0 | 1 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0002t0003 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0002t0005 | 0/0 | 3256 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0002t0006 | 0/1 | 3256 | 1 | 0 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0002t0007 | 0/0 | 3256 | 4 | 0 | 0 | 0 | 0 | 4 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0005t0001 | 0/0 | 3256 | 8 | 8 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0006t0001 | 0/0 | 3256 | 4 | 0 | 0 | 4 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0007t0001 | 0/0 | 3256 | 3 | 3 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0010t0001 | 0/0 | 3256 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0011t0001 | 0/0 | 3256 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0021t0001 | 0/0 | 3256 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0025t0001 | 0/0 | 3256 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0002c0026t0001 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0003c0019t0001 | 0/0 | 3256 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0004c0018t0003 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0005c0014t0001 | 0/0 | 3256 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0006c0013t0001 | 0/0 | 3256 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0007c0016t0001 | 0/0 | 3256 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0008c0023t0003 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0009c0024t0001 | 0/0 | 3256 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| a0010c0022t0001 | 0/0 | 3256 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | copy fasta | chr12 | 125060435 | 125148316 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0006g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0001t0011g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0003t0009g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0004t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0008t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0009t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0009t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0012t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0015t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0017t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0001c0020t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0006g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0007g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0007g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0002t0007g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0005t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0006t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0006t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0007t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0007t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0010t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0011t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0021t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0025t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0002c0026t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0003c0019t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0004c0018t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0005c0014t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0006c0013t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0007c0016t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0008c0023t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0009c0024t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| a0010c0022t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0198 | EUR | GBR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | GBR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0063 | EUR | GBR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | GBR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0220 | EUR | FIN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00544 | hp2 | a0001 | c0004 | t0004 | g0249 | EAS | CHS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00558 | hp2 | a0001 | c0020 | t0002 | g0173 | EAS | CHS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0226 | EAS | CHS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00597 | hp2 | a0001 | c0004 | t0004 | g0246 | EAS | CHS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00621 | hp1 | a0001 | c0003 | t0009 | g0189 | EAS | CHS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | CHS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0224 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00738 | hp1 | a0010 | c0022 | t0001 | g0128 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0084 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0292 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0336 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01175 | hp2 | a0002 | c0025 | t0001 | g0255 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01243 | hp2 | a0005 | c0014 | t0001 | g0339 | AMR | PUR | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0064 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0186 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0272 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0270 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0273 | EUR | IBS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0192 | EUR | IBS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0274 | EUR | IBS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0206 | EUR | IBS | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01884 | hp1 | a0002 | c0005 | t0001 | g0023 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01891 | hp1 | a0002 | c0005 | t0001 | g0024 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0324 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0105 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0110 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0106 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0308 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02015 | hp2 | a0001 | c0008 | t0001 | g0211 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02040 | hp2 | a0001 | c0004 | t0004 | g0241 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0256 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0236 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02132 | hp2 | a0001 | c0004 | t0004 | g0254 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02148 | hp1 | a0001 | c0001 | t0011 | g0108 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | CDX | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CDX | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02165 | hp1 | a0001 | c0004 | t0004 | g0167 | EAS | CDX | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CDX | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0354 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0107 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02280 | hp1 | a0002 | c0007 | t0001 | g0016 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0310 | AMR | PEL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0262 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02451 | hp2 | a0002 | c0011 | t0001 | g0014 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0160 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0267 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0212 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02630 | hp2 | a0002 | c0005 | t0001 | g0022 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0359 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0199 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02717 | hp1 | a0006 | c0013 | t0001 | g0350 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0053 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0264 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02723 | hp2 | a0002 | c0005 | t0001 | g0020 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02895 | hp2 | a0001 | c0009 | t0001 | g0349 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02897 | hp2 | a0001 | c0009 | t0001 | g0348 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02922 | hp1 | a0002 | c0005 | t0001 | g0025 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02970 | hp1 | a0002 | c0005 | t0001 | g0019 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03041 | hp2 | a0002 | c0002 | t0005 | g0096 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03139 | hp1 | a0001 | c0015 | t0001 | g0070 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03139 | hp2 | a0002 | c0021 | t0001 | g0026 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0355 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03486 | hp2 | a0002 | c0010 | t0001 | g0018 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03491 | hp2 | a0002 | c0002 | t0007 | g0113 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03492 | hp2 | a0002 | c0002 | t0007 | g0112 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03669 | hp2 | a0001 | c0001 | t0010 | g0194 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | STU | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03704 | hp2 | a0002 | c0002 | t0007 | g0146 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | BEB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0353 | SAS | BEB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG04184 | hp1 | a0001 | c0003 | t0004 | g0083 | SAS | BEB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG04184 | hp2 | a0002 | c0002 | t0007 | g0279 | SAS | BEB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG04204 | hp2 | a0003 | c0019 | t0001 | g0184 | SAS | STU | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | YRI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | CHB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18906 | hp1 | a0009 | c0024 | t0001 | g0263 | AFR | YRI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18939 | hp2 | a0008 | c0023 | t0003 | g0119 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18951 | hp2 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18954 | hp2 | a0002 | c0006 | t0001 | g0122 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18957 | hp1 | a0001 | c0017 | t0002 | g0204 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18966 | hp1 | a0001 | c0004 | t0004 | g0209 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18967 | hp1 | a0004 | c0018 | t0003 | g0280 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18967 | hp2 | a0002 | c0006 | t0001 | g0149 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0216 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18975 | hp2 | a0001 | c0012 | t0004 | g0244 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18977 | hp2 | a0001 | c0004 | t0004 | g0250 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18984 | hp2 | a0002 | c0002 | t0003 | g0120 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18989 | hp2 | a0001 | c0004 | t0004 | g0242 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18992 | hp1 | a0001 | c0004 | t0004 | g0328 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19004 | hp1 | a0002 | c0006 | t0001 | g0123 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19004 | hp2 | a0001 | c0008 | t0002 | g0238 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19007 | hp1 | a0001 | c0004 | t0004 | g0243 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19010 | hp2 | a0001 | c0004 | t0004 | g0245 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19012 | hp1 | a0002 | c0006 | t0001 | g0138 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0213 | AFR | LWK | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | LWK | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19055 | hp1 | a0001 | c0004 | t0004 | g0237 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19060 | hp1 | a0001 | c0004 | t0004 | g0098 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0342 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19066 | hp2 | a0002 | c0026 | t0001 | g0145 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0338 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA19240 | hp2 | a0007 | c0016 | t0001 | g0032 | AFR | YRI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ASW | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0076 | EUR | TSI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | TSI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0197 | EUR | TSI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0092 | EUR | TSI | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | GIH | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02109 | hp2 | a0002 | c0005 | t0001 | g0015 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02486 | hp2 | a0002 | c0005 | t0001 | g0021 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03471 | hp1 | a0002 | c0007 | t0001 | g0017 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG06807 | hp1 | a0002 | c0007 | t0001 | g0027 | AFR | USA | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18955 | hp1 | a0001 | c0004 | t0004 | g0341 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0346 | AFR | USA | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0006 | g0136 | REF | REF | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0052 | REF | REF | AACS_chr12_125060435_125148316 | AACS | chr12 | 125060435 | 125148316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:125076605
|
A | G | 4 | a0002a0008a0009others(1): Show | 86 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(83): Show |
missense_variant | MODERATE | c.352A>G | p.Ile118Val | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/18 | 502/3256 | 352/2019 | 118/672 | chr12 | 125076605 | ||
| chr12:125107252
|
T | G | 1 | a0010 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.899T>G | p.Met300Arg | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/18 | 1049/3256 | 899/2019 | 300/672 | chr12 | 125107252 | ||
| chr12:125114478
|
G | A | 1 | a0008 | 1 | NA18939.hp2 | missense_variant&splice_region_variant | MODERATE | c.917G>A | p.Gly306Asp | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/18 | 1067/3256 | 917/2019 | 306/672 | chr12 | 125114478 | ||
| chr12:125124908
|
C | T | 1 | a0003 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1193C>T | p.Thr398Ile | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/18 | 1343/3256 | 1193/2019 | 398/672 | chr12 | 125124908 | ||
| chr12:125124913
|
A | T | 1 | a0004 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1198A>T | p.Ser400Cys | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/18 | 1348/3256 | 1198/2019 | 400/672 | chr12 | 125124913 | ||
| chr12:125128260
|
C | T | 1 | a0007 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1409C>T | p.Ala470Val | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/18 | 1559/3256 | 1409/2019 | 470/672 | chr12 | 125128260 | ||
| chr12:125134805
|
T | C | 1 | a0006 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1631T>C | p.Leu544Pro | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/18 | 1781/3256 | 1631/2019 | 544/672 | chr12 | 125134805 | ||
| chr12:125136673
|
G | C | 2 | a0005a0009 | 2 | HG01243.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.1690G>C | p.Glu564Gln | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/18 | 1840/3256 | 1690/2019 | 564/672 | chr12 | 125136673 | ||
| chr12:125143315
|
C | T | 1 | a0002 | 4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
splice_region_variant | LOW | c.*1086C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | chr12 | 125143315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:125076572
|
C | A | 3 | a0002c0005a0002c0010a0002c0011 | 10 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.319C>A | p.Arg107Arg | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/18 | 469/3256 | 319/2019 | 107/672 | chr12 | 125076572 | ||
| chr12:125102732
|
G | A | 4 | a0001c0004a0001c0008a0001c0012others(1): Show | 20 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(17): Show |
synonymous_variant | LOW | c.624G>A | p.Glu208Glu | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 6/18 | 774/3256 | 624/2019 | 208/672 | chr12 | 125102732 | ||
| chr12:125107181
|
C | T | 1 | a0001c0020 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.828C>T | p.Phe276Phe | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/18 | 978/3256 | 828/2019 | 276/672 | chr12 | 125107181 | ||
| chr12:125107238
|
C | T | 1 | a0002c0006 | 4 | NA18954.hp2 NA18967.hp2 NA19004.hp1 others(1): Show |
synonymous_variant | LOW | c.885C>T | p.Gly295Gly | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/18 | 1035/3256 | 885/2019 | 295/672 | chr12 | 125107238 | ||
| chr12:125125005
|
C | T | 1 | a0002c0011 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1290C>T | p.Ile430Ile | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/18 | 1440/3256 | 1290/2019 | 430/672 | chr12 | 125125005 | ||
| chr12:125128174
|
C | T | 1 | a0001c0017 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.1323C>T | p.Ile441Ile | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/18 | 1473/3256 | 1323/2019 | 441/672 | chr12 | 125128174 | ||
| chr12:125134046
|
C | T | 1 | a0001c0009 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.1593C>T | p.Thr531Thr | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 15/18 | 1743/3256 | 1593/2019 | 531/672 | chr12 | 125134046 | ||
| chr12:125134836
|
G | A | 1 | a0002c0007 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.1662G>A | p.Ser554Ser | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/18 | 1812/3256 | 1662/2019 | 554/672 | chr12 | 125134836 | ||
| chr12:125136738
|
C | T | 1 | a0001c0012 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.1755C>T | p.Leu585Leu | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/18 | 1905/3256 | 1755/2019 | 585/672 | chr12 | 125136738 | ||
| chr12:125142139
|
C | T | 6 | a0001c0003a0001c0004a0001c0012others(3): Show | 43 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(40): Show |
synonymous_variant | LOW | c.1929C>T | p.Ile643Ile | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | 2079/3256 | 1929/2019 | 643/672 | chr12 | 125142139 | ||
| chr12:125142175
|
G | A | 3 | a0001c0015a0002c0010a0002c0025 | 3 | HG01175.hp2 HG03139.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.1965G>A | p.Ser655Ser | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | 2115/3256 | 1965/2019 | 655/672 | chr12 | 125142175 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:125065473
|
C | T | 1 | a0001c0001t0011 | 1 | HG02148.hp1 | 5_prime_UTR_variant | MODIFIER | c.-112C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/18 | 112 | chr12 | 125065473 | |||||
| chr12:125065500
|
C | T | 1 | a0001c0001t0010 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/18 | 85 | chr12 | 125065500 | |||||
| chr12:125065521
|
C | T | 1 | a0001c0003t0009 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-64C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/18 | 64 | chr12 | 125065521 | |||||
| chr12:125142239
|
G | C | 5 | a0001c0001t0003a0001c0001t0008a0002c0002t0003others(2): Show | 25 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*10G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | 10 | chr12 | 125142239 | |||||
| chr12:125142507
|
C | T | 7 | a0001c0001t0002a0001c0001t0010a0001c0008t0002others(4): Show | 79 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*278C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | 278 | chr12 | 125142507 | |||||
| chr12:125142641
|
C | T | 3 | a0001c0001t0005a0001c0001t0011a0002c0002t0005 | 15 | HG00140.hp1 HG01515.hp2 HG01928.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*412C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | 412 | chr12 | 125142641 | |||||
| chr12:125142786
|
A | G | 2 | a0001c0001t0006a0002c0002t0006 | 12 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*557A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | 557 | chr12 | 125142786 | |||||
| chr12:125142788
|
G | A | 1 | a0001c0001t0008 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*559G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | 559 | chr12 | 125142788 | |||||
| chr12:125143177
|
C | A | 3 | a0001c0003t0004a0001c0004t0004a0001c0012t0004 | 16 | HG00544.hp2 HG00597.hp2 HG02040.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*948C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 18/18 | 948 | chr12 | 125143177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:125065757
|
C | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.133+40C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125065757 | ||||||
| chr12:125065898
|
C | T | 15 | a0001c0001t0001g0028a0002c0005t0001g0015a0002c0005t0001g0019others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+181C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125065898 | ||||||
| chr12:125066060
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.133+343G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066060 | ||||||
| chr12:125066138
|
A | G | 1 | a0002c0002t0002g0359 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.133+421A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066138 | ||||||
| chr12:125066151
|
C | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0356others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+434C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066151 | ||||||
| chr12:125066187
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0007c0016t0001g0032 | 3 | HG02257.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133+470G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066187 | ||||||
| chr12:125066450
|
A | AT | 172 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(169): Show | 175 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.133+751dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125066450 | |||||
| chr12:125066450
|
A | ATT | 86 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(83): Show | 88 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.133+750_133+751dup others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125066450 | |||||
| chr12:125066450
|
A | ATTT | 13 | a0001c0001t0001g0013a0001c0001t0001g0343a0001c0001t0001g0345others(10): Show | 13 | HG02055.hp2 HG02135.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.133+749_133+751dup others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125066450 | |||||
| chr12:125066450
|
AT | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG01243.hp1 HG01975.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+751delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125066450 | |||||
| chr12:125066518
|
C | T | 1 | a0001c0003t0001g0342 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.133+801C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066518 | ||||||
| chr12:125066637
|
C | T | 1 | a0002c0021t0001g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.133+920C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066637 | ||||||
| chr12:125066692
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.133+975G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066692 | ||||||
| chr12:125066738
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.133+1021G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066738 | ||||||
| chr12:125066793
|
C | T | 5 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+1076C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066793 | ||||||
| chr12:125066969
|
C | A | 1 | a0001c0001t0002g0101 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.133+1252C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066969 | ||||||
| chr12:125066999
|
T | G | 3 | a0001c0001t0001g0358a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.133+1282T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125066999 | ||||||
| chr12:125067012
|
A | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(109): Show | 114 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+1295A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125067012 | ||||||
| chr12:125067214
|
C | T | 1 | a0001c0003t0001g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.133+1497C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125067214 | ||||||
| chr12:125067282
|
G | T | 1 | a0001c0001t0005g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.133+1565G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125067282 | ||||||
| chr12:125067542
|
A | AT | 6 | a0001c0004t0004g0098a0002c0002t0001g0006a0002c0002t0001g0007others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+1839dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125067542 | |||||
| chr12:125067542
|
AT | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(190): Show | 197 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.133+1839delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125067542 | |||||
| chr12:125067634
|
C | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0097a0001c0001t0001g0275others(72): Show | 76 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.133+1917C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125067634 | ||||||
| chr12:125067786
|
G | A | 1 | a0004c0018t0003g0280 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.133+2069G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125067786 | ||||||
| chr12:125067834
|
G | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0097a0001c0001t0001g0275others(72): Show | 76 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.133+2117G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125067834 | ||||||
| chr12:125067842
|
G | A | 1 | a0002c0002t0001g0102 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.133+2125G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125067842 | ||||||
| chr12:125067995
|
G | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.133+2278G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125067995 | ||||||
| chr12:125068010
|
G | T | 1 | a0001c0001t0001g0333 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.133+2293G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068010 | ||||||
| chr12:125068034
|
C | T | 54 | a0002c0002t0001g0001a0002c0002t0001g0102a0002c0002t0001g0111others(51): Show | 55 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.133+2317C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068034 | ||||||
| chr12:125068128
|
C | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(199): Show | 206 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(203): Show |
intron_variant | MODIFIER | c.133+2411C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068128 | ||||||
| chr12:125068319
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(276): Show | 284 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.133+2602T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068319 | ||||||
| chr12:125068342
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0257a0005c0014t0001g0339 | 4 | HG01243.hp2 HG02145.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+2625C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068342 | ||||||
| chr12:125068364
|
T | C | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(274): Show | 282 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.133+2647T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068364 | ||||||
| chr12:125068369
|
G | A | 1 | a0001c0001t0001g0333 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.133+2652G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068369 | ||||||
| chr12:125068407
|
C | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0333 | 3 | HG00558.hp1 NA18955.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.133+2690C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068407 | ||||||
| chr12:125068425
|
C | G | 10 | a0002c0005t0001g0015a0002c0005t0001g0019a0002c0005t0001g0020others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+2708C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068425 | ||||||
| chr12:125068843
|
CT | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.133+3140delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125068843 | |||||
| chr12:125068900
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(137): Show | 143 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.133+3183C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068900 | ||||||
| chr12:125068969
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02922.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.133+3252A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068969 | ||||||
| chr12:125068985
|
ATGCAACA others(5): Show |
A | 1 | a0001c0001t0001g0333 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.133+3269_133+3280d others(14): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125068985 | ||||||
| chr12:125069052
|
A | G | 54 | a0002c0002t0001g0001a0002c0002t0001g0102a0002c0002t0001g0111others(51): Show | 55 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.133+3335A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069052 | ||||||
| chr12:125069092
|
C | A | 1 | a0002c0002t0002g0359 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.133+3375C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069092 | ||||||
| chr12:125069115
|
A | T | 10 | a0002c0005t0001g0015a0002c0005t0001g0019a0002c0005t0001g0020others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+3398A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069115 | ||||||
| chr12:125069117
|
A | T | 10 | a0002c0005t0001g0015a0002c0005t0001g0019a0002c0005t0001g0020others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+3400A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069117 | ||||||
| chr12:125069133
|
G | C | 1 | a0001c0001t0002g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.133+3416G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069133 | ||||||
| chr12:125069259
|
C | T | 5 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3542C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069259 | ||||||
| chr12:125069273
|
G | C | 54 | a0002c0002t0001g0001a0002c0002t0001g0102a0002c0002t0001g0111others(51): Show | 55 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.133+3556G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069273 | ||||||
| chr12:125069356
|
G | A | 12 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(9): Show | 12 | HG02040.hp1 HG03834.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+3639G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069356 | ||||||
| chr12:125069396
|
T | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.133+3679T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069396 | ||||||
| chr12:125069763
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.133+4046G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069763 | ||||||
| chr12:125069809
|
A | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0281others(67): Show | 71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.134-4067A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069809 | ||||||
| chr12:125069918
|
A | T | 1 | a0001c0003t0001g0256 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.134-3958A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069918 | ||||||
| chr12:125069920
|
T | C | 10 | a0002c0005t0001g0015a0002c0005t0001g0019a0002c0005t0001g0020others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-3956T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069920 | ||||||
| chr12:125069974
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0281others(140): Show | 146 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.134-3902A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125069974 | ||||||
| chr12:125070042
|
C | T | 1 | a0005c0014t0001g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.134-3834C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070042 | ||||||
| chr12:125070112
|
G | A | 1 | a0009c0024t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-3764G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070112 | ||||||
| chr12:125070168
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.134-3708C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070168 | ||||||
| chr12:125070348
|
G | T | 1 | a0001c0004t0004g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.134-3528G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070348 | ||||||
| chr12:125070353
|
C | T | 1 | a0002c0002t0001g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.134-3523C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070353 | ||||||
| chr12:125070558
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 8 | HG01243.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-3318G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070558 | ||||||
| chr12:125070576
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.134-3300G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070576 | ||||||
| chr12:125070624
|
A | G | 1 | a0001c0001t0002g0155 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.134-3252A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070624 | ||||||
| chr12:125070679
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.134-3197G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070679 | ||||||
| chr12:125070692
|
C | T | 1 | a0001c0001t0003g0330 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.134-3184C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070692 | ||||||
| chr12:125070693
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0030others(158): Show | 165 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.134-3183A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070693 | ||||||
| chr12:125070705
|
T | A | 1 | a0001c0001t0002g0156 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.134-3171T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070705 | ||||||
| chr12:125070752
|
G | A | 115 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0100others(112): Show | 116 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.134-3124G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070752 | ||||||
| chr12:125070767
|
A | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0281others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.134-3109A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070767 | ||||||
| chr12:125070767
|
A | G | 1 | a0001c0003t0001g0353 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.134-3109A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070767 | ||||||
| chr12:125070786
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0257a0002c0002t0001g0006others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-3090C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070786 | ||||||
| chr12:125070882
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.134-2994A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070882 | ||||||
| chr12:125070916
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0281others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.134-2960G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070916 | ||||||
| chr12:125070923
|
G | A | 74 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0102others(71): Show | 76 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.134-2953G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125070923 | ||||||
| chr12:125071097
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.134-2779C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071097 | ||||||
| chr12:125071170
|
A | G | 2 | a0002c0002t0001g0273a0002c0002t0001g0274 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.134-2706A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071170 | ||||||
| chr12:125071486
|
A | C | 3 | a0001c0001t0001g0358a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.134-2390A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071486 | ||||||
| chr12:125071534
|
C | G | 1 | a0001c0004t0004g0328 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.134-2342C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071534 | ||||||
| chr12:125071725
|
C | G | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.134-2151C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071725 | ||||||
| chr12:125071732
|
G | T | 55 | a0002c0002t0001g0001a0002c0002t0001g0102a0002c0002t0001g0111others(52): Show | 56 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.134-2144G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071732 | ||||||
| chr12:125071795
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134-2081A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071795 | ||||||
| chr12:125071807
|
G | A | 1 | a0002c0021t0001g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.134-2069G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071807 | ||||||
| chr12:125071879
|
CAG | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0030others(79): Show | 84 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1994_134-1993d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125071879 | |||||
| chr12:125071927
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02922.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.134-1949G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125071927 | ||||||
| chr12:125072006
|
C | T | 1 | a0002c0002t0001g0150 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.134-1870C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072006 | ||||||
| chr12:125072157
|
C | CT | 81 | a0001c0001t0001g0005a0001c0001t0001g0251a0001c0001t0001g0275others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.134-1704dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125072157 | |||||
| chr12:125072157
|
C | CTT | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(9): Show | 12 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-1705_134-1704d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125072157 | |||||
| chr12:125072357
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.134-1519C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072357 | ||||||
| chr12:125072376
|
G | A | 5 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 5 | HG02922.hp2 HG03453.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-1500G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072376 | ||||||
| chr12:125072399
|
C | T | 1 | a0002c0002t0001g0272 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.134-1477C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072399 | ||||||
| chr12:125072426
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.134-1450A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072426 | ||||||
| chr12:125072485
|
C | T | 348 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(345): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.134-1391C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072485 | ||||||
| chr12:125072486
|
C | T | 1 | a0001c0004t0004g0328 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.134-1390C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072486 | ||||||
| chr12:125072527
|
A | T | 1 | a0001c0003t0001g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.134-1349A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072527 | ||||||
| chr12:125072827
|
C | G | 1 | a0001c0003t0001g0256 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.134-1049C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072827 | ||||||
| chr12:125072830
|
A | G | 1 | a0005c0014t0001g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.134-1046A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072830 | ||||||
| chr12:125072847
|
G | A | 1 | a0001c0001t0005g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.134-1029G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072847 | ||||||
| chr12:125072885
|
T | G | 16 | a0002c0002t0001g0004a0002c0002t0001g0264a0002c0002t0001g0265others(13): Show | 17 | HG01361.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.134-991T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072885 | ||||||
| chr12:125072887
|
A | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.134-989A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072887 | ||||||
| chr12:125072905
|
A | G | 2 | a0001c0001t0006g0084a0001c0001t0006g0160 | 2 | HG00741.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.134-971A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072905 | ||||||
| chr12:125072918
|
TG | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-957delG | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072918 | ||||||
| chr12:125072919
|
G | GT | 12 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0078others(9): Show | 12 | HG01109.hp1 HG01168.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.134-931dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125072919 | |||||
| chr12:125072919
|
GT | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0097others(33): Show | 36 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.134-931delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125072919 | |||||
| chr12:125072919
|
GTT | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0028others(168): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.134-932_134-931del others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125072919 | |||||
| chr12:125072919
|
GTTT | G | 70 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0333others(67): Show | 72 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.134-933_134-931del others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 125072919 | |||||
| chr12:125072926
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.134-950T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072926 | ||||||
| chr12:125072926
|
T | G | 1 | a0001c0001t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.134-950T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072926 | ||||||
| chr12:125072927
|
T | G | 1 | a0001c0004t0004g0328 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.134-949T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072927 | ||||||
| chr12:125072928
|
T | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(69): Show | 73 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.134-948T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072928 | ||||||
| chr12:125072929
|
T | G | 1 | a0001c0001t0001g0333 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.134-947T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072929 | ||||||
| chr12:125072930
|
T | G | 1 | a0002c0021t0001g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.134-946T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072930 | ||||||
| chr12:125072933
|
T | G | 1 | a0001c0004t0004g0328 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.134-943T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072933 | ||||||
| chr12:125072934
|
T | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0281others(65): Show | 69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.134-942T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072934 | ||||||
| chr12:125072935
|
T | G | 1 | a0001c0001t0001g0333 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.134-941T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072935 | ||||||
| chr12:125072950
|
T | C | 282 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(279): Show | 287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.134-926T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125072950 | ||||||
| chr12:125073118
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.134-758T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125073118 | ||||||
| chr12:125073127
|
A | G | 1 | a0002c0002t0005g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.134-749A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125073127 | ||||||
| chr12:125073163
|
G | C | 276 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0028others(273): Show | 281 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.134-713G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125073163 | ||||||
| chr12:125073270
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134-606A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125073270 | ||||||
| chr12:125073460
|
C | G | 1 | a0001c0001t0002g0047 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.134-416C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125073460 | ||||||
| chr12:125073733
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.134-143A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125073733 | ||||||
| chr12:125073820
|
T | A | 3 | a0001c0001t0001g0358a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.134-56T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 1/17 | chr12 | 125073820 | ||||||
| chr12:125073997
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.237+18G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125073997 | ||||||
| chr12:125074062
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(5): Show | 9 | HG00733.hp1 HG01081.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.237+83T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074062 | ||||||
| chr12:125074063
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.237+84G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074063 | ||||||
| chr12:125074155
|
C | T | 1 | a0002c0002t0001g0272 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.237+176C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074155 | ||||||
| chr12:125074461
|
T | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(9): Show | 13 | HG00733.hp1 HG01081.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.237+482T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074461 | ||||||
| chr12:125074504
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.237+525G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074504 | ||||||
| chr12:125074557
|
G | A | 79 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0006others(76): Show | 81 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.237+578G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074557 | ||||||
| chr12:125074638
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.237+659T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074638 | ||||||
| chr12:125074651
|
A | G | 3 | a0001c0001t0001g0358a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.237+672A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074651 | ||||||
| chr12:125074660
|
G | GT | 46 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(43): Show | 47 | HG01109.hp2 HG01175.hp2 HG01258.hp2 others(44): Show |
intron_variant | MODIFIER | c.237+702dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 125074660 | |||||
| chr12:125074660
|
G | GTT | 9 | a0001c0001t0001g0097a0001c0001t0001g0277a0001c0001t0001g0278others(6): Show | 9 | HG00733.hp1 HG01081.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.237+701_237+702dup others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 125074660 | |||||
| chr12:125074670
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.237+691T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074670 | ||||||
| chr12:125074737
|
T | C | 1 | a0001c0001t0002g0286 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.237+758T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074737 | ||||||
| chr12:125074825
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.237+846G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074825 | ||||||
| chr12:125074911
|
G | A | 3 | a0001c0001t0001g0358a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.237+932G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074911 | ||||||
| chr12:125074956
|
G | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(71): Show | 75 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.237+977G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125074956 | ||||||
| chr12:125074975
|
G | GT | 129 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(126): Show | 131 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.237+1014dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 125074975 | |||||
| chr12:125074975
|
G | GTT | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0002g0101others(3): Show | 6 | HG00733.hp1 HG01081.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.237+1013_237+1014d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 125074975 | |||||
| chr12:125075044
|
G | A | 1 | a0001c0001t0003g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.237+1065G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075044 | ||||||
| chr12:125075131
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.237+1152C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075131 | ||||||
| chr12:125075155
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0335 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.237+1176A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075155 | ||||||
| chr12:125075276
|
G | A | 14 | a0001c0001t0001g0172a0001c0001t0002g0101a0001c0001t0002g0165others(11): Show | 14 | HG00558.hp2 HG02015.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.238-1215G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075276 | ||||||
| chr12:125075346
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.238-1145G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075346 | ||||||
| chr12:125075523
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0257a0005c0014t0001g0339 | 4 | HG01243.hp2 HG02145.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-968C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075523 | ||||||
| chr12:125075534
|
C | T | 114 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0097others(111): Show | 115 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.238-957C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075534 | ||||||
| chr12:125075590
|
C | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0257a0005c0014t0001g0339 | 4 | HG01243.hp2 HG02145.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-901C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075590 | ||||||
| chr12:125075595
|
G | GT | 26 | a0001c0001t0001g0038a0001c0001t0001g0227a0001c0001t0001g0284others(23): Show | 26 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.238-880dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 125075595 | |||||
| chr12:125075648
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0257a0005c0014t0001g0339 | 4 | HG01243.hp2 HG02145.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-843C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075648 | ||||||
| chr12:125075722
|
C | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0281others(67): Show | 71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.238-769C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075722 | ||||||
| chr12:125075725
|
C | T | 1 | a0001c0003t0001g0353 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.238-766C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075725 | ||||||
| chr12:125075738
|
C | T | 1 | a0001c0003t0001g0225 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.238-753C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075738 | ||||||
| chr12:125075796
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.238-695G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075796 | ||||||
| chr12:125075828
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.238-663G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075828 | ||||||
| chr12:125075996
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0231 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.238-495C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125075996 | ||||||
| chr12:125076148
|
C | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0336 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.238-343C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125076148 | ||||||
| chr12:125076150
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.238-341C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125076150 | ||||||
| chr12:125076174
|
A | T | 114 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0097others(111): Show | 115 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.238-317A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125076174 | ||||||
| chr12:125076203
|
T | A | 83 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0006others(80): Show | 85 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.238-288T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125076203 | ||||||
| chr12:125076400
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.238-91C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 2/17 | chr12 | 125076400 | ||||||
| chr12:125076646
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.358+35G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125076646 | ||||||
| chr12:125076656
|
T | C | 2 | a0002c0002t0001g0111a0002c0002t0001g0267 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.358+45T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125076656 | ||||||
| chr12:125076682
|
A | T | 1 | a0001c0004t0004g0246 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.358+71A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125076682 | ||||||
| chr12:125076739
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+128G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125076739 | ||||||
| chr12:125076749
|
G | A | 5 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 5 | HG02896.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+138G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125076749 | ||||||
| chr12:125076976
|
T | G | 1 | a0001c0004t0004g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.358+365T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125076976 | ||||||
| chr12:125076988
|
G | A | 53 | a0002c0002t0001g0001a0002c0002t0001g0102a0002c0002t0001g0111others(50): Show | 54 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.358+377G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125076988 | ||||||
| chr12:125077003
|
G | T | 1 | a0001c0001t0002g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.358+392G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077003 | ||||||
| chr12:125077012
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.358+401A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077012 | ||||||
| chr12:125077074
|
A | AT | 17 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(14): Show | 17 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.358+484dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125077074 | |||||
| chr12:125077074
|
AT | A | 113 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0097others(110): Show | 114 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.358+484delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125077074 | |||||
| chr12:125077285
|
C | T | 2 | a0002c0002t0001g0001a0002c0002t0001g0268 | 3 | HG01891.hp2 HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.358+674C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077285 | ||||||
| chr12:125077338
|
G | A | 1 | a0001c0001t0006g0224 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.358+727G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077338 | ||||||
| chr12:125077347
|
G | A | 4 | a0002c0002t0007g0112a0002c0002t0007g0113a0002c0002t0007g0146others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+736G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077347 | ||||||
| chr12:125077359
|
T | A | 4 | a0002c0002t0007g0112a0002c0002t0007g0113a0002c0002t0007g0146others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+748T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077359 | ||||||
| chr12:125077367
|
A | G | 4 | a0002c0002t0007g0112a0002c0002t0007g0113a0002c0002t0007g0146others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+756A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077367 | ||||||
| chr12:125077435
|
A | G | 6 | a0001c0001t0001g0228a0001c0001t0001g0258a0001c0001t0001g0259others(3): Show | 6 | HG00642.hp1 HG02735.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+824A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077435 | ||||||
| chr12:125077494
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0257a0005c0014t0001g0339 | 4 | HG01243.hp2 HG02145.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+883A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077494 | ||||||
| chr12:125077499
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0257a0005c0014t0001g0339 | 4 | HG01243.hp2 HG02145.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+888G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077499 | ||||||
| chr12:125077509
|
C | CA | 14 | a0001c0001t0001g0061a0001c0001t0001g0333a0001c0001t0001g0351others(11): Show | 14 | HG00741.hp2 HG01106.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.358+916dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125077509 | |||||
| chr12:125077509
|
CA | C | 7 | a0001c0001t0003g0314a0001c0003t0001g0221a0002c0002t0001g0132others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+916delA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125077509 | |||||
| chr12:125077534
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.358+923G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077534 | ||||||
| chr12:125077585
|
T | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(71): Show | 75 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.358+974T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077585 | ||||||
| chr12:125077621
|
C | G | 114 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0097others(111): Show | 115 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.358+1010C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077621 | ||||||
| chr12:125077707
|
C | A | 1 | a0001c0001t0005g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.358+1096C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077707 | ||||||
| chr12:125077717
|
A | AT | 16 | a0001c0001t0001g0159a0001c0001t0001g0277a0001c0001t0001g0278others(13): Show | 16 | HG00733.hp1 HG00733.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+1120dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125077717 | |||||
| chr12:125077866
|
T | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG00733.hp1 HG01081.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+1255T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077866 | ||||||
| chr12:125077883
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.358+1272A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077883 | ||||||
| chr12:125077936
|
T | C | 1 | a0002c0002t0001g0141 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.358+1325T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077936 | ||||||
| chr12:125077943
|
A | T | 1 | a0002c0021t0001g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.358+1332A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077943 | ||||||
| chr12:125077987
|
G | T | 1 | a0001c0001t0006g0084 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.358+1376G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077987 | ||||||
| chr12:125077989
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+1378C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125077989 | ||||||
| chr12:125078006
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+1395G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078006 | ||||||
| chr12:125078238
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(71): Show | 75 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.358+1627C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078238 | ||||||
| chr12:125078263
|
G | A | 350 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(347): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.358+1652G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078263 | ||||||
| chr12:125078346
|
C | T | 53 | a0002c0002t0001g0001a0002c0002t0001g0102a0002c0002t0001g0111others(50): Show | 54 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.358+1735C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078346 | ||||||
| chr12:125078420
|
T | G | 286 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.358+1809T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078420 | ||||||
| chr12:125078475
|
T | G | 1 | a0002c0010t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.358+1864T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078475 | ||||||
| chr12:125078592
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.358+1981G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078592 | ||||||
| chr12:125078689
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+2078T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078689 | ||||||
| chr12:125078820
|
C | CA | 67 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(64): Show | 69 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.358+2234dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125078820 | |||||
| chr12:125078820
|
C | CAA | 15 | a0001c0001t0001g0162a0001c0001t0005g0048a0002c0002t0001g0114others(12): Show | 15 | HG00621.hp2 HG01433.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.358+2233_358+2234d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125078820 | |||||
| chr12:125078820
|
CA | C | 114 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(111): Show | 115 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.358+2234delA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125078820 | |||||
| chr12:125078820
|
CAA | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0281others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.358+2233_358+2234d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125078820 | |||||
| chr12:125078871
|
C | T | 83 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0006others(80): Show | 85 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.358+2260C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078871 | ||||||
| chr12:125078885
|
C | T | 1 | a0001c0003t0001g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.358+2274C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125078885 | ||||||
| chr12:125079018
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+2407A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079018 | ||||||
| chr12:125079086
|
G | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.358+2475G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079086 | ||||||
| chr12:125079108
|
C | T | 83 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0006others(80): Show | 85 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.358+2497C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079108 | ||||||
| chr12:125079391
|
G | A | 1 | a0002c0002t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358+2780G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079391 | ||||||
| chr12:125079408
|
G | A | 1 | a0001c0001t0002g0321 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.358+2797G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079408 | ||||||
| chr12:125079589
|
A | C | 1 | a0002c0002t0001g0141 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.358+2978A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079589 | ||||||
| chr12:125079608
|
C | T | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.358+2997C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079608 | ||||||
| chr12:125079609
|
G | A | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.358+2998G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079609 | ||||||
| chr12:125079614
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+3003C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079614 | ||||||
| chr12:125079678
|
T | C | 286 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.358+3067T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079678 | ||||||
| chr12:125079692
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+3081T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079692 | ||||||
| chr12:125079693
|
C | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+3082C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079693 | ||||||
| chr12:125079731
|
A | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+3120A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079731 | ||||||
| chr12:125079789
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.358+3178G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079789 | ||||||
| chr12:125079817
|
C | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0281others(67): Show | 71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.358+3206C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079817 | ||||||
| chr12:125079874
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.358+3263C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079874 | ||||||
| chr12:125079999
|
C | G | 3 | a0001c0001t0001g0327a0001c0001t0003g0320a0001c0001t0003g0330 | 3 | NA18964.hp2 NA19067.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.358+3388C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125079999 | ||||||
| chr12:125080102
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.358+3491C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080102 | ||||||
| chr12:125080181
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.358+3570G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080181 | ||||||
| chr12:125080201
|
G | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(72): Show | 77 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.358+3590G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080201 | ||||||
| chr12:125080212
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+3601G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080212 | ||||||
| chr12:125080297
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+3686A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080297 | ||||||
| chr12:125080307
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.358+3696C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080307 | ||||||
| chr12:125080338
|
AAAACCCA others(13): Show |
A | 1 | a0001c0004t0004g0237 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.358+3745_358+3764d others(22): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125080338 | |||||
| chr12:125080406
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.358+3795C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080406 | ||||||
| chr12:125080470
|
G | GTC | 81 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 83 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.358+3877_358+3878d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125080470 | |||||
| chr12:125080470
|
G | GTCTC | 6 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0131others(3): Show | 6 | NA18939.hp2 NA18944.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+3875_358+3878d others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125080470 | |||||
| chr12:125080494
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG00733.hp1 HG01081.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+3883C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080494 | ||||||
| chr12:125080641
|
C | CTT | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.358+4031_358+4032d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125080641 | |||||
| chr12:125080657
|
C | CA | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+4046_358+4047i others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080657 | ||||||
| chr12:125080760
|
C | T | 2 | a0001c0001t0003g0313a0002c0021t0001g0026 | 2 | HG02273.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.358+4149C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080760 | ||||||
| chr12:125080840
|
C | G | 83 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0006others(80): Show | 85 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.358+4229C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080840 | ||||||
| chr12:125080840
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+4229C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080840 | ||||||
| chr12:125080852
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+4241T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080852 | ||||||
| chr12:125080865
|
G | T | 83 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0006others(80): Show | 85 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.358+4254G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080865 | ||||||
| chr12:125080881
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+4270T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080881 | ||||||
| chr12:125080913
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+4302C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125080913 | ||||||
| chr12:125081082
|
T | C | 4 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(1): Show | 4 | HG02145.hp1 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4471T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081082 | ||||||
| chr12:125081117
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+4506T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081117 | ||||||
| chr12:125081136
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+4525G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081136 | ||||||
| chr12:125081141
|
C | T | 114 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0097others(111): Show | 115 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.358+4530C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081141 | ||||||
| chr12:125081142
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG00733.hp1 HG01081.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.358+4531G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081142 | ||||||
| chr12:125081166
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+4555A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081166 | ||||||
| chr12:125081228
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.358+4617A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081228 | ||||||
| chr12:125081273
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0005g0103others(1): Show | 4 | HG02257.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4662C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081273 | ||||||
| chr12:125081278
|
A | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0005g0103others(1): Show | 4 | HG02257.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4667A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081278 | ||||||
| chr12:125081386
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.358+4775G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081386 | ||||||
| chr12:125081404
|
A | G | 156 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(153): Show | 159 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.358+4793A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081404 | ||||||
| chr12:125081512
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.359-4818G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081512 | ||||||
| chr12:125081776
|
G | T | 1 | a0001c0001t0002g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.359-4554G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081776 | ||||||
| chr12:125081842
|
C | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02055.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.359-4488C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081842 | ||||||
| chr12:125081845
|
G | A | 83 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0006others(80): Show | 85 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.359-4485G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081845 | ||||||
| chr12:125081858
|
C | CAAATAGG others(28): Show |
1 | a0001c0001t0002g0081 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.359-4470_359-4436d others(37): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125081858 | |||||
| chr12:125081879
|
G | GT | 7 | a0001c0001t0001g0013a0001c0001t0001g0227a0001c0001t0002g0183others(4): Show | 7 | HG00735.hp2 HG02055.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-4438dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125081879 | |||||
| chr12:125081915
|
G | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(114): Show | 119 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.359-4415G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125081915 | ||||||
| chr12:125082171
|
AT | A | 343 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(340): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.359-4142delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125082171 | |||||
| chr12:125082208
|
G | C | 83 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0006others(80): Show | 85 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.359-4122G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082208 | ||||||
| chr12:125082342
|
AT | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0002g0037others(2): Show | 6 | HG02040.hp1 HG03490.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-3973delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125082342 | |||||
| chr12:125082357
|
T | A | 62 | a0001c0001t0001g0029a0001c0001t0001g0100a0001c0001t0001g0169others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.359-3973T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082357 | ||||||
| chr12:125082395
|
C | T | 24 | a0002c0002t0001g0004a0002c0002t0001g0036a0002c0002t0001g0094others(21): Show | 25 | HG01243.hp1 HG01361.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.359-3935C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082395 | ||||||
| chr12:125082429
|
G | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.359-3901G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082429 | ||||||
| chr12:125082513
|
G | A | 1 | a0005c0014t0001g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.359-3817G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082513 | ||||||
| chr12:125082566
|
AT | A | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.359-3763delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082566 | ||||||
| chr12:125082637
|
A | G | 61 | a0001c0001t0001g0029a0001c0001t0001g0100a0001c0001t0001g0169others(58): Show | 62 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.359-3693A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082637 | ||||||
| chr12:125082691
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.359-3639G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082691 | ||||||
| chr12:125082830
|
C | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0335 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.359-3500C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125082830 | ||||||
| chr12:125082832
|
G | GAC | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0005g0103others(2): Show | 5 | HG01175.hp2 HG02257.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-3482_359-3481d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125082832 | |||||
| chr12:125083023
|
A | G | 84 | a0001c0001t0001g0337a0002c0002t0001g0001a0002c0002t0001g0004others(81): Show | 86 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.359-3307A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083023 | ||||||
| chr12:125083207
|
C | T | 199 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0097others(196): Show | 202 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.359-3123C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083207 | ||||||
| chr12:125083232
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.359-3098C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083232 | ||||||
| chr12:125083243
|
G | C | 85 | a0001c0001t0001g0337a0001c0001t0002g0321a0002c0002t0001g0001others(82): Show | 87 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.359-3087G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083243 | ||||||
| chr12:125083333
|
A | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(276): Show | 284 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.359-2997A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083333 | ||||||
| chr12:125083425
|
C | CT | 70 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0281others(67): Show | 71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.359-2904dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125083425 | |||||
| chr12:125083432
|
G | A | 3 | a0001c0001t0001g0358a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.359-2898G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083432 | ||||||
| chr12:125083577
|
G | C | 2 | a0001c0001t0005g0063a0001c0001t0006g0064 | 2 | HG00140.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.359-2753G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083577 | ||||||
| chr12:125083615
|
A | T | 1 | a0001c0001t0002g0252 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.359-2715A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083615 | ||||||
| chr12:125083821
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.359-2509G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083821 | ||||||
| chr12:125083950
|
G | A | 1 | a0001c0001t0002g0344 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.359-2380G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125083950 | ||||||
| chr12:125084099
|
C | G | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.359-2231C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084099 | ||||||
| chr12:125084100
|
A | G | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.359-2230A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084100 | ||||||
| chr12:125084183
|
G | A | 2 | a0002c0002t0001g0273a0002c0002t0001g0274 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.359-2147G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084183 | ||||||
| chr12:125084249
|
C | T | 1 | a0001c0001t0005g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.359-2081C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084249 | ||||||
| chr12:125084317
|
C | CA | 77 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(74): Show | 78 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.359-2002dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125084317 | |||||
| chr12:125084395
|
C | T | 2 | a0001c0001t0006g0084a0001c0001t0006g0160 | 2 | HG00741.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.359-1935C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084395 | ||||||
| chr12:125084442
|
T | G | 117 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0097others(114): Show | 118 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.359-1888T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084442 | ||||||
| chr12:125084578
|
AT | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(151): Show | 157 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.359-1736delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125084578 | |||||
| chr12:125084594
|
T | C | 1 | a0001c0001t0003g0326 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.359-1736T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084594 | ||||||
| chr12:125084684
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.359-1646T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084684 | ||||||
| chr12:125084771
|
C | T | 13 | a0001c0003t0001g0354a0001c0003t0001g0355a0002c0002t0001g0006others(10): Show | 13 | HG01175.hp2 HG01243.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.359-1559C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084771 | ||||||
| chr12:125084801
|
C | T | 3 | a0001c0001t0002g0316a0001c0001t0002g0347a0001c0004t0004g0328 | 3 | HG02135.hp1 NA18992.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.359-1529C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084801 | ||||||
| chr12:125084821
|
A | T | 7 | a0001c0003t0001g0354a0001c0003t0001g0355a0002c0002t0001g0036others(4): Show | 7 | HG01243.hp1 HG02258.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-1509A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125084821 | ||||||
| chr12:125085041
|
A | G | 10 | a0002c0005t0001g0015a0002c0005t0001g0019a0002c0005t0001g0020others(7): Show | 10 | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.359-1289A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085041 | ||||||
| chr12:125085071
|
C | T | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.359-1259C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085071 | ||||||
| chr12:125085127
|
G | C | 1 | a0002c0002t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.359-1203G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085127 | ||||||
| chr12:125085167
|
T | C | 93 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0001t0001g0191others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.359-1163T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085167 | ||||||
| chr12:125085249
|
T | C | 109 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0028others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.359-1081T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085249 | ||||||
| chr12:125085307
|
C | G | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359-1023C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085307 | ||||||
| chr12:125085393
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(10): Show | 14 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.359-937C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085393 | ||||||
| chr12:125085394
|
G | A | 3 | a0002c0002t0001g0004a0002c0002t0001g0264a0005c0014t0001g0339 | 4 | HG01243.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-936G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085394 | ||||||
| chr12:125085408
|
G | A | 5 | a0001c0001t0002g0040a0001c0001t0002g0155a0001c0001t0002g0302others(2): Show | 5 | NA18941.hp1 NA18984.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-922G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085408 | ||||||
| chr12:125085414
|
C | G | 5 | a0001c0001t0002g0040a0001c0001t0002g0155a0001c0001t0002g0302others(2): Show | 5 | NA18941.hp1 NA18984.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-916C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085414 | ||||||
| chr12:125085425
|
G | A | 5 | a0001c0001t0002g0040a0001c0001t0002g0155a0001c0001t0002g0302others(2): Show | 5 | NA18941.hp1 NA18984.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-905G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085425 | ||||||
| chr12:125085427
|
C | G | 5 | a0001c0001t0002g0040a0001c0001t0002g0155a0001c0001t0002g0302others(2): Show | 5 | NA18941.hp1 NA18984.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-903C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085427 | ||||||
| chr12:125085434
|
A | G | 5 | a0001c0001t0002g0040a0001c0001t0002g0155a0001c0001t0002g0302others(2): Show | 5 | NA18941.hp1 NA18984.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-896A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085434 | ||||||
| chr12:125085464
|
C | T | 55 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0100others(52): Show | 56 | HG00621.hp2 HG00642.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.359-866C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085464 | ||||||
| chr12:125085474
|
GTGGAACC others(33): Show |
G | 1 | a0001c0001t0001g0332 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.359-846_359-807del others(40): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 125085474 | |||||
| chr12:125085514
|
A | G | 348 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(345): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.359-816A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085514 | ||||||
| chr12:125085523
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.359-807C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085523 | ||||||
| chr12:125085549
|
G | C | 1 | a0001c0003t0001g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.359-781G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085549 | ||||||
| chr12:125085599
|
A | G | 1 | a0001c0001t0002g0182 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.359-731A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085599 | ||||||
| chr12:125085630
|
T | C | 138 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(135): Show | 140 | HG00140.hp1 HG00621.hp2 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.359-700T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085630 | ||||||
| chr12:125085651
|
C | T | 333 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(330): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.359-679C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085651 | ||||||
| chr12:125085681
|
C | A | 349 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(346): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.359-649C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085681 | ||||||
| chr12:125085808
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.359-522G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085808 | ||||||
| chr12:125085891
|
C | T | 3 | a0002c0002t0007g0112a0002c0002t0007g0113a0002c0002t0007g0146 | 3 | HG03491.hp2 HG03492.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.359-439C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085891 | ||||||
| chr12:125085892
|
G | A | 30 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0080others(27): Show | 30 | HG00140.hp1 HG00741.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.359-438G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125085892 | ||||||
| chr12:125086086
|
G | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-244G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 3/17 | chr12 | 125086086 | ||||||
| chr12:125086452
|
T | C | 2 | a0001c0001t0001g0079a0002c0002t0001g0075 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.472+9T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125086452 | ||||||
| chr12:125086818
|
A | G | 52 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(49): Show | 53 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.472+375A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125086818 | ||||||
| chr12:125087023
|
C | T | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.472+580C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087023 | ||||||
| chr12:125087147
|
C | T | 1 | a0002c0002t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.472+704C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087147 | ||||||
| chr12:125087234
|
G | T | 1 | a0001c0001t0003g0292 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.472+791G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087234 | ||||||
| chr12:125087333
|
C | A | 2 | a0002c0002t0001g0117a0002c0002t0001g0118 | 2 | NA18944.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.472+890C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087333 | ||||||
| chr12:125087333
|
C | T | 64 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0161others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.472+890C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087333 | ||||||
| chr12:125087491
|
C | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+1048C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087491 | ||||||
| chr12:125087542
|
C | T | 2 | a0001c0001t0002g0071a0001c0001t0002g0082 | 2 | HG02165.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.472+1099C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087542 | ||||||
| chr12:125087576
|
C | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+1133C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087576 | ||||||
| chr12:125087630
|
C | T | 4 | a0001c0003t0001g0210a0001c0003t0001g0221a0001c0003t0001g0225others(1): Show | 4 | HG02155.hp1 NA18942.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+1187C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087630 | ||||||
| chr12:125087642
|
G | C | 2 | a0001c0001t0001g0079a0002c0002t0001g0075 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.472+1199G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087642 | ||||||
| chr12:125087646
|
G | A | 3 | a0002c0002t0001g0008a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG03471.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.472+1203G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087646 | ||||||
| chr12:125087665
|
G | A | 1 | a0002c0002t0001g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.472+1222G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087665 | ||||||
| chr12:125087776
|
G | A | 1 | a0002c0002t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.472+1333G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087776 | ||||||
| chr12:125087937
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.472+1494G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087937 | ||||||
| chr12:125087974
|
C | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.472+1531C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087974 | ||||||
| chr12:125087991
|
C | T | 15 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0042others(12): Show | 15 | HG02040.hp1 HG02129.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.472+1548C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125087991 | ||||||
| chr12:125088017
|
A | T | 3 | a0002c0002t0001g0008a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG03471.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.472+1574A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088017 | ||||||
| chr12:125088217
|
G | C | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.472+1774G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088217 | ||||||
| chr12:125088224
|
C | CT | 14 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0002others(11): Show | 15 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.472+1800dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 125088224 | |||||
| chr12:125088224
|
CT | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0159others(33): Show | 36 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.472+1800delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 125088224 | |||||
| chr12:125088285
|
G | A | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+1842G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088285 | ||||||
| chr12:125088317
|
C | T | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.472+1874C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088317 | ||||||
| chr12:125088321
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.472+1878C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088321 | ||||||
| chr12:125088336
|
G | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0239others(20): Show | 23 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.472+1893G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088336 | ||||||
| chr12:125088379
|
C | T | 4 | a0001c0003t0001g0354a0001c0003t0001g0355a0002c0002t0001g0036others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+1936C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088379 | ||||||
| chr12:125088380
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.472+1937G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088380 | ||||||
| chr12:125088433
|
A | G | 3 | a0002c0002t0001g0008a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG03471.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.472+1990A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088433 | ||||||
| chr12:125088524
|
C | T | 200 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0030others(197): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.472+2081C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088524 | ||||||
| chr12:125088729
|
T | C | 31 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0080others(28): Show | 31 | HG00140.hp1 HG00741.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.472+2286T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088729 | ||||||
| chr12:125088775
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.472+2332C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088775 | ||||||
| chr12:125088825
|
C | T | 64 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0161others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.472+2382C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088825 | ||||||
| chr12:125088975
|
C | T | 2 | a0001c0001t0001g0079a0002c0002t0001g0075 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.473-2451C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088975 | ||||||
| chr12:125088991
|
C | T | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.473-2435C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125088991 | ||||||
| chr12:125089023
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.473-2403G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089023 | ||||||
| chr12:125089061
|
C | T | 26 | a0001c0001t0001g0327a0001c0001t0003g0041a0001c0001t0003g0044others(23): Show | 26 | HG01099.hp1 HG01123.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.473-2365C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089061 | ||||||
| chr12:125089145
|
G | A | 6 | a0001c0001t0003g0179a0002c0002t0001g0121a0002c0002t0001g0130others(3): Show | 6 | HG00621.hp2 NA18954.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.473-2281G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089145 | ||||||
| chr12:125089159
|
C | T | 9 | a0002c0005t0001g0015a0002c0005t0001g0019a0002c0005t0001g0020others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.473-2267C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089159 | ||||||
| chr12:125089254
|
C | G | 51 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0100others(48): Show | 51 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.473-2172C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089254 | ||||||
| chr12:125089290
|
G | C | 8 | a0001c0001t0001g0097a0002c0002t0001g0124a0002c0002t0001g0137others(5): Show | 8 | HG01361.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-2136G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089290 | ||||||
| chr12:125089377
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-2049T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089377 | ||||||
| chr12:125089392
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.473-2034C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089392 | ||||||
| chr12:125089422
|
C | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0336 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.473-2004C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089422 | ||||||
| chr12:125089428
|
G | A | 1 | a0001c0003t0001g0342 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.473-1998G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089428 | ||||||
| chr12:125089661
|
C | A | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.473-1765C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089661 | ||||||
| chr12:125089738
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.473-1688C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089738 | ||||||
| chr12:125089919
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.473-1507A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089919 | ||||||
| chr12:125089927
|
A | G | 1 | a0002c0002t0001g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.473-1499A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089927 | ||||||
| chr12:125089979
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.473-1447A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089979 | ||||||
| chr12:125089979
|
A | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-1447A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125089979 | ||||||
| chr12:125090069
|
T | G | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.473-1357T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090069 | ||||||
| chr12:125090139
|
ACC | A | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1286_473-1285d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090139 | ||||||
| chr12:125090142
|
A | T | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1284A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090142 | ||||||
| chr12:125090168
|
CT | C | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1257delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090168 | ||||||
| chr12:125090189
|
C | T | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1237C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090189 | ||||||
| chr12:125090191
|
T | C | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1235T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090191 | ||||||
| chr12:125090197
|
C | T | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1229C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090197 | ||||||
| chr12:125090207
|
T | TCATCCAT others(127): Show |
1 | a0001c0001t0002g0231 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.473-1219_473-1218i others(136): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090207 | ||||||
| chr12:125090207
|
T | TCATCCAT others(145): Show |
353 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(350): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.473-1219_473-1218i others(154): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090207 | ||||||
| chr12:125090207
|
T | TCATCCAT others(149): Show |
1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.473-1219_473-1218i others(158): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090207 | ||||||
| chr12:125090207
|
T | TCATCCAT others(141): Show |
2 | a0002c0002t0001g0273a0002c0002t0001g0274 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.473-1219_473-1218i others(150): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090207 | ||||||
| chr12:125090207
|
T | TCATCCAT others(143): Show |
1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.473-1219_473-1218i others(152): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090207 | ||||||
| chr12:125090208
|
T | C | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1218T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090208 | ||||||
| chr12:125090216
|
T | C | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1210T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090216 | ||||||
| chr12:125090228
|
T | C | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1198T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090228 | ||||||
| chr12:125090230
|
T | TC | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1196_473-1195i others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090230 | ||||||
| chr12:125090233
|
TG | T | 358 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(355): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.473-1192delG | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090233 | ||||||
| chr12:125090305
|
C | G | 1 | a0001c0001t0003g0312 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.473-1121C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090305 | ||||||
| chr12:125090318
|
CAACT | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-1107_473-1104d others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090318 | ||||||
| chr12:125090690
|
T | A | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.473-736T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090690 | ||||||
| chr12:125090691
|
CCATCCAT others(25): Show |
C | 12 | a0001c0001t0001g0010a0001c0015t0001g0070a0002c0005t0001g0015others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.473-725_473-694del others(32): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 125090691 | |||||
| chr12:125090723
|
TCATC | T | 3 | a0001c0001t0001g0284a0001c0001t0001g0300a0001c0001t0001g0345 | 3 | NA18943.hp2 NA18952.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.473-686_473-683del others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 125090723 | |||||
| chr12:125090750
|
C | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-676C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090750 | ||||||
| chr12:125090861
|
C | T | 4 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0229others(1): Show | 4 | HG01192.hp1 HG01433.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-565C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090861 | ||||||
| chr12:125090893
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.473-533G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125090893 | ||||||
| chr12:125091027
|
C | G | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.473-399C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125091027 | ||||||
| chr12:125091136
|
G | A | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0239others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.473-290G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125091136 | ||||||
| chr12:125091203
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.473-223C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125091203 | ||||||
| chr12:125091288
|
G | T | 1 | a0001c0001t0001g0329 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.473-138G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125091288 | ||||||
| chr12:125091347
|
C | G | 1 | a0001c0001t0005g0063 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.473-79C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125091347 | ||||||
| chr12:125091383
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.473-43A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 4/17 | chr12 | 125091383 | ||||||
| chr12:125091961
|
C | T | 8 | a0001c0001t0001g0097a0002c0002t0001g0124a0002c0002t0001g0137others(5): Show | 8 | HG01361.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+438C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125091961 | ||||||
| chr12:125091969
|
G | A | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.570+446G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125091969 | ||||||
| chr12:125092098
|
C | G | 1 | a0002c0005t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.570+575C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092098 | ||||||
| chr12:125092101
|
A | G | 1 | a0001c0003t0001g0353 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.570+578A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092101 | ||||||
| chr12:125092114
|
C | T | 9 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 9 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+591C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092114 | ||||||
| chr12:125092126
|
A | C | 1 | a0001c0001t0002g0303 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.570+603A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092126 | ||||||
| chr12:125092227
|
A | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02922.hp2 HG03453.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+704A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092227 | ||||||
| chr12:125092263
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.570+740C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092263 | ||||||
| chr12:125092437
|
T | G | 3 | a0002c0002t0001g0008a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG03471.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.570+914T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092437 | ||||||
| chr12:125092556
|
A | G | 3 | a0002c0002t0001g0008a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG03471.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.570+1033A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092556 | ||||||
| chr12:125092625
|
C | G | 1 | a0001c0001t0002g0347 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.570+1102C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092625 | ||||||
| chr12:125092643
|
G | A | 3 | a0002c0002t0001g0008a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG03471.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.570+1120G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092643 | ||||||
| chr12:125092705
|
C | A | 1 | a0001c0001t0001g0284 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.570+1182C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092705 | ||||||
| chr12:125092708
|
G | A | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1185G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092708 | ||||||
| chr12:125092725
|
T | TG | 340 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(337): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.570+1202_570+1203i others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092725 | ||||||
| chr12:125092846
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 10 | HG02145.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+1323C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092846 | ||||||
| chr12:125092941
|
C | T | 4 | a0001c0003t0001g0354a0001c0003t0001g0355a0002c0002t0001g0036others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+1418C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125092941 | ||||||
| chr12:125093040
|
G | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0239others(20): Show | 23 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.570+1517G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093040 | ||||||
| chr12:125093077
|
GC | G | 21 | a0001c0001t0001g0307a0001c0001t0002g0182a0001c0003t0001g0168others(18): Show | 21 | HG00597.hp1 HG00621.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.570+1556delC | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125093077 | |||||
| chr12:125093149
|
G | C | 1 | a0002c0002t0003g0120 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.570+1626G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093149 | ||||||
| chr12:125093188
|
C | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0039others(75): Show | 80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.570+1665C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093188 | ||||||
| chr12:125093235
|
T | C | 2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.570+1712T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093235 | ||||||
| chr12:125093380
|
G | GACCCCAG others(16): Show |
1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.570+1859_570+1881d others(25): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125093380 | |||||
| chr12:125093424
|
T | C | 1 | a0002c0002t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.570+1901T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093424 | ||||||
| chr12:125093488
|
C | G | 2 | a0001c0004t0001g0212a0001c0004t0001g0213 | 2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.570+1965C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093488 | ||||||
| chr12:125093508
|
G | A | 3 | a0001c0001t0005g0060a0001c0001t0005g0072a0001c0001t0005g0099 | 3 | HG02630.hp1 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.570+1985G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093508 | ||||||
| chr12:125093590
|
C | T | 1 | a0001c0017t0002g0204 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.570+2067C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093590 | ||||||
| chr12:125093736
|
C | T | 1 | a0001c0001t0003g0292 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.570+2213C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093736 | ||||||
| chr12:125093746
|
A | G | 8 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01243.hp1 HG02258.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+2223A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093746 | ||||||
| chr12:125093749
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.570+2226T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093749 | ||||||
| chr12:125093789
|
A | C | 1 | a0001c0004t0004g0328 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.570+2266A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093789 | ||||||
| chr12:125093824
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.570+2301C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093824 | ||||||
| chr12:125093873
|
T | G | 2 | a0001c0001t0003g0044a0001c0001t0008g0208 | 2 | NA18612.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.570+2350T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093873 | ||||||
| chr12:125093926
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+2403T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093926 | ||||||
| chr12:125093991
|
T | C | 1 | a0005c0014t0001g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.570+2468T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125093991 | ||||||
| chr12:125094039
|
C | T | 2 | a0002c0002t0001g0114a0002c0002t0001g0139 | 2 | NA18950.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.570+2516C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094039 | ||||||
| chr12:125094125
|
G | T | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.570+2602G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094125 | ||||||
| chr12:125094126
|
T | G | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.570+2603T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094126 | ||||||
| chr12:125094216
|
T | C | 340 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(337): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.570+2693T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094216 | ||||||
| chr12:125094466
|
G | T | 1 | a0001c0001t0001g0315 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.570+2943G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094466 | ||||||
| chr12:125094487
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.570+2964C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094487 | ||||||
| chr12:125094547
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.570+3024G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094547 | ||||||
| chr12:125094650
|
T | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 10 | HG01243.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+3127T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094650 | ||||||
| chr12:125094683
|
C | T | 2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.570+3160C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094683 | ||||||
| chr12:125094972
|
G | C | 20 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0239others(17): Show | 20 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.570+3449G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094972 | ||||||
| chr12:125094972
|
G | T | 2 | a0001c0004t0001g0212a0001c0004t0001g0213 | 2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.570+3449G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125094972 | ||||||
| chr12:125094978
|
CGTGT | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0203a0001c0001t0002g0187others(1): Show | 4 | HG02970.hp1 HG03688.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+3498_570+3501d others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125094978
|
CGTGTGT | C | 46 | a0001c0001t0001g0077a0001c0001t0001g0091a0001c0001t0001g0093others(43): Show | 46 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.570+3496_570+3501d others(8): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125094978
|
CGTGTGTG others(1): Show |
C | 83 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0050others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.570+3494_570+3501d others(10): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125094978
|
CGTGTGTG others(3): Show |
C | 14 | a0001c0001t0001g0003a0001c0001t0002g0002a0001c0001t0002g0166others(11): Show | 17 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.570+3492_570+3501d others(12): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125094978
|
CGTGTGTG others(5): Show |
C | 6 | a0001c0001t0001g0010a0001c0004t0004g0209a0001c0004t0004g0241others(3): Show | 6 | HG02040.hp2 HG03139.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+3490_570+3501d others(14): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125094978
|
CGTGTGTG others(7): Show |
C | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0079others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+3488_570+3501d others(16): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125094978
|
CGTGTGTG others(9): Show |
C | 164 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0030others(161): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.570+3486_570+3501d others(18): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125094978
|
CGTGTGTG others(11): Show |
C | 22 | a0001c0001t0001g0315a0001c0001t0001g0327a0001c0001t0003g0041others(19): Show | 22 | HG01099.hp1 HG01123.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.570+3484_570+3501d others(20): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125094978
|
CGTGTGTG others(15): Show |
C | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | NA18950.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.570+3480_570+3501d others(24): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125094978 | |||||
| chr12:125095011
|
G | C | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.570+3488G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095011 | ||||||
| chr12:125095017
|
G | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0239others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.570+3494G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095017 | ||||||
| chr12:125095020
|
TGTGTCTG others(4): Show |
T | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.570+3498_570+3508d others(13): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095020 | ||||||
| chr12:125095134
|
A | G | 193 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0030others(190): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.570+3611A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095134 | ||||||
| chr12:125095514
|
C | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 10 | HG01243.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+3991C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095514 | ||||||
| chr12:125095565
|
G | A | 2 | a0001c0001t0002g0071a0001c0001t0002g0082 | 2 | HG02165.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.570+4042G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095565 | ||||||
| chr12:125095588
|
C | T | 9 | a0001c0001t0002g0200a0001c0001t0002g0220a0001c0001t0006g0186others(6): Show | 9 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+4065C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095588 | ||||||
| chr12:125095652
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0039others(108): Show | 114 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.570+4129C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095652 | ||||||
| chr12:125095981
|
C | A | 10 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 10 | HG01243.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+4458C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095981 | ||||||
| chr12:125095988
|
G | A | 16 | a0001c0004t0004g0098a0001c0004t0004g0167a0001c0004t0004g0209others(13): Show | 16 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+4465G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125095988 | ||||||
| chr12:125096462
|
C | T | 3 | a0001c0009t0001g0348a0001c0009t0001g0349a0006c0013t0001g0350 | 3 | HG02717.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.570+4939C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125096462 | ||||||
| chr12:125096734
|
C | A | 15 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0042others(12): Show | 15 | HG02040.hp1 HG02129.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.570+5211C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125096734 | ||||||
| chr12:125096797
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG03239.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+5274C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125096797 | ||||||
| chr12:125096895
|
C | T | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0301 | 3 | NA18950.hp2 NA19007.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.570+5372C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125096895 | ||||||
| chr12:125096906
|
G | A | 7 | a0001c0001t0001g0172a0002c0002t0001g0117a0002c0002t0001g0118others(4): Show | 7 | NA18939.hp2 NA18944.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+5383G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125096906 | ||||||
| chr12:125096950
|
C | T | 8 | a0001c0001t0002g0182a0001c0003t0001g0168a0001c0003t0001g0216others(5): Show | 8 | HG00597.hp1 HG02071.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+5427C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125096950 | ||||||
| chr12:125097002
|
G | C | 1 | a0001c0001t0008g0208 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.570+5479G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097002 | ||||||
| chr12:125097082
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.570+5559C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097082 | ||||||
| chr12:125097153
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.571-5526C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097153 | ||||||
| chr12:125097203
|
A | G | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.571-5476A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097203 | ||||||
| chr12:125097239
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-5440A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097239 | ||||||
| chr12:125097433
|
T | TA | 75 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0161others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.571-5229dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125097433 | |||||
| chr12:125097433
|
TA | T | 22 | a0001c0001t0001g0079a0001c0001t0001g0159a0001c0001t0001g0162others(19): Show | 22 | HG00733.hp1 HG00733.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.571-5229delA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125097433 | |||||
| chr12:125097521
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0157 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.571-5158G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097521 | ||||||
| chr12:125097652
|
G | T | 337 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.571-5027G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097652 | ||||||
| chr12:125097708
|
C | T | 2 | a0001c0003t0001g0354a0001c0003t0001g0355 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.571-4971C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097708 | ||||||
| chr12:125097845
|
C | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0030others(187): Show | 192 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.571-4834C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097845 | ||||||
| chr12:125097847
|
C | T | 1 | a0002c0002t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.571-4832C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097847 | ||||||
| chr12:125097877
|
C | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0239others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.571-4802C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097877 | ||||||
| chr12:125097937
|
G | A | 1 | a0001c0001t0006g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.571-4742G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097937 | ||||||
| chr12:125097962
|
G | A | 1 | a0001c0020t0002g0173 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.571-4717G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097962 | ||||||
| chr12:125097970
|
G | T | 1 | a0001c0003t0001g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571-4709G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125097970 | ||||||
| chr12:125098142
|
T | C | 2 | a0001c0001t0001g0079a0002c0002t0001g0075 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.571-4537T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098142 | ||||||
| chr12:125098195
|
A | T | 7 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-4484A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098195 | ||||||
| chr12:125098200
|
C | T | 1 | a0002c0002t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.571-4479C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098200 | ||||||
| chr12:125098284
|
G | C | 49 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0100others(46): Show | 49 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.571-4395G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098284 | ||||||
| chr12:125098316
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.571-4363G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098316 | ||||||
| chr12:125098393
|
A | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0239others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.571-4286A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098393 | ||||||
| chr12:125098405
|
A | AG | 9 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 10 | HG02145.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-4274_571-4273i others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098405 | ||||||
| chr12:125098453
|
C | CT | 6 | a0001c0001t0001g0010a0001c0001t0005g0110a0001c0003t0001g0262others(3): Show | 6 | HG01978.hp1 HG02451.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-4212dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125098453 | |||||
| chr12:125098601
|
G | A | 10 | a0001c0001t0001g0261a0002c0005t0001g0015a0002c0005t0001g0019others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-4078G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098601 | ||||||
| chr12:125098617
|
A | G | 4 | a0001c0003t0001g0354a0001c0003t0001g0355a0002c0002t0001g0036others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-4062A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098617 | ||||||
| chr12:125098626
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.571-4053A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098626 | ||||||
| chr12:125098679
|
T | C | 1 | a0001c0003t0001g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.571-4000T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098679 | ||||||
| chr12:125098713
|
G | A | 348 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(345): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.571-3966G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098713 | ||||||
| chr12:125098714
|
G | A | 191 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(188): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.571-3965G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098714 | ||||||
| chr12:125098849
|
A | G | 1 | a0002c0002t0006g0136 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.571-3830A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098849 | ||||||
| chr12:125098986
|
G | A | 9 | a0002c0005t0001g0015a0002c0005t0001g0019a0002c0005t0001g0020others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-3693G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125098986 | ||||||
| chr12:125099003
|
C | A | 43 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(40): Show | 44 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.571-3676C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099003 | ||||||
| chr12:125099033
|
C | T | 1 | a0002c0002t0001g0001 | 2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.571-3646C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099033 | ||||||
| chr12:125099044
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.571-3635G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099044 | ||||||
| chr12:125099244
|
G | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0239others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.571-3435G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099244 | ||||||
| chr12:125099437
|
T | G | 1 | a0001c0003t0001g0256 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.571-3242T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099437 | ||||||
| chr12:125099515
|
G | T | 7 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02486.hp1 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3164G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099515 | ||||||
| chr12:125099545
|
G | A | 16 | a0001c0004t0004g0098a0001c0004t0004g0167a0001c0004t0004g0209others(13): Show | 16 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.571-3134G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099545 | ||||||
| chr12:125099593
|
G | C | 1 | a0009c0024t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.571-3086G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099593 | ||||||
| chr12:125099609
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.571-3070C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099609 | ||||||
| chr12:125099718
|
G | A | 5 | a0001c0004t0004g0237a0001c0004t0004g0242a0001c0004t0004g0243others(2): Show | 5 | NA18955.hp1 NA18977.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-2961G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099718 | ||||||
| chr12:125099796
|
C | T | 192 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.571-2883C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099796 | ||||||
| chr12:125099956
|
G | A | 2 | a0001c0009t0001g0348a0001c0009t0001g0349 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.571-2723G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099956 | ||||||
| chr12:125099976
|
G | A | 1 | a0002c0002t0001g0148 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.571-2703G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125099976 | ||||||
| chr12:125100152
|
A | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0231 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.571-2527A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100152 | ||||||
| chr12:125100204
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.571-2475C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100204 | ||||||
| chr12:125100386
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.571-2293T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100386 | ||||||
| chr12:125100436
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 10 | HG02145.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-2243C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100436 | ||||||
| chr12:125100457
|
G | T | 4 | a0001c0003t0001g0354a0001c0003t0001g0355a0002c0002t0001g0036others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-2222G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100457 | ||||||
| chr12:125100712
|
C | T | 1 | a0001c0001t0002g0302 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.571-1967C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100712 | ||||||
| chr12:125100893
|
C | T | 5 | a0001c0001t0001g0287a0002c0002t0001g0011a0002c0002t0001g0273others(2): Show | 5 | HG01175.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-1786C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100893 | ||||||
| chr12:125100910
|
A | T | 1 | a0001c0001t0005g0063 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.571-1769A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100910 | ||||||
| chr12:125100946
|
G | A | 1 | a0001c0001t0002g0082 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.571-1733G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100946 | ||||||
| chr12:125100960
|
G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0077others(13): Show | 16 | HG01515.hp2 HG01928.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.571-1719G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125100960 | ||||||
| chr12:125101008
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.571-1671G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101008 | ||||||
| chr12:125101076
|
C | T | 1 | a0001c0001t0006g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.571-1603C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101076 | ||||||
| chr12:125101099
|
C | T | 2 | a0001c0001t0001g0287a0002c0025t0001g0255 | 2 | HG01175.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.571-1580C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101099 | ||||||
| chr12:125101146
|
C | A | 38 | a0001c0001t0001g0077a0001c0001t0001g0097a0001c0001t0001g0159others(35): Show | 39 | HG00733.hp2 HG01243.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.571-1533C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101146 | ||||||
| chr12:125101350
|
G | A | 2 | a0001c0003t0001g0168a0001c0003t0001g0216 | 2 | NA18962.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.571-1329G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101350 | ||||||
| chr12:125101350
|
G | T | 4 | a0001c0003t0001g0053a0001c0003t0001g0354a0001c0003t0001g0355others(1): Show | 4 | HG02258.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1329G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101350 | ||||||
| chr12:125101381
|
A | G | 1 | a0005c0014t0001g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.571-1298A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101381 | ||||||
| chr12:125101396
|
C | G | 1 | a0001c0001t0002g0178 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.571-1283C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101396 | ||||||
| chr12:125101547
|
G | A | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(24): Show | 28 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.571-1132G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101547 | ||||||
| chr12:125101732
|
G | C | 2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.571-947G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101732 | ||||||
| chr12:125101762
|
C | CT | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(298): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.571-895dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125101762 | |||||
| chr12:125101762
|
C | CTT | 34 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0196others(31): Show | 34 | HG00597.hp1 HG00597.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.571-896_571-895dup others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125101762 | |||||
| chr12:125101925
|
C | A | 1 | a0001c0001t0002g0183 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.571-754C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125101925 | ||||||
| chr12:125102059
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(181): Show | 187 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.571-620T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102059 | ||||||
| chr12:125102068
|
T | TA | 125 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(122): Show | 127 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.571-600dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125102068 | |||||
| chr12:125102068
|
T | TTA | 17 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0340others(14): Show | 17 | HG01515.hp2 HG01928.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.571-611_571-610ins others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102068 | ||||||
| chr12:125102068
|
T | TTAA | 5 | a0001c0001t0005g0104a0002c0002t0001g0004a0002c0002t0001g0264others(2): Show | 6 | HG01243.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-611_571-610ins others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102068 | ||||||
| chr12:125102068
|
T | TTAAA | 9 | a0001c0001t0001g0097a0001c0001t0001g0159a0002c0002t0001g0011others(6): Show | 9 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-611_571-610ins others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102068 | ||||||
| chr12:125102068
|
T | TTTA | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0005g0048others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-611_571-610ins others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102068 | ||||||
| chr12:125102069
|
A | T | 3 | a0001c0001t0001g0327a0001c0001t0003g0320a0001c0001t0003g0330 | 3 | NA18964.hp2 NA19067.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.571-610A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102069 | ||||||
| chr12:125102079
|
A | AAC | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(11): Show | 14 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.571-600_571-599ins others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102079 | ||||||
| chr12:125102080
|
C | A | 42 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(39): Show | 43 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.571-599C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102080 | ||||||
| chr12:125102080
|
C | CA | 14 | a0001c0001t0001g0077a0001c0001t0001g0340a0001c0001t0001g0356others(11): Show | 14 | HG01515.hp2 HG01928.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.571-589dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 125102080 | |||||
| chr12:125102091
|
C | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(181): Show | 187 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.571-588C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102091 | ||||||
| chr12:125102105
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.571-574G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102105 | ||||||
| chr12:125102325
|
C | T | 1 | a0002c0002t0001g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.571-354C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102325 | ||||||
| chr12:125102342
|
G | A | 21 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(18): Show | 22 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.571-337G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102342 | ||||||
| chr12:125102345
|
C | T | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.571-334C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102345 | ||||||
| chr12:125102431
|
G | A | 2 | a0002c0002t0001g0273a0002c0002t0001g0274 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.571-248G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102431 | ||||||
| chr12:125102479
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(156): Show | 161 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.571-200T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102479 | ||||||
| chr12:125102495
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.571-184C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 5/17 | chr12 | 125102495 | ||||||
| chr12:125102932
|
G | GA | 10 | a0001c0001t0001g0079a0001c0001t0001g0352a0001c0001t0005g0060others(7): Show | 10 | HG00621.hp1 HG00621.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.686-56dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 125102932 | |||||
| chr12:125103160
|
T | C | 127 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.767+79T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103160 | ||||||
| chr12:125103230
|
A | G | 22 | a0001c0001t0001g0287a0001c0004t0001g0212a0001c0004t0001g0213others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.767+149A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103230 | ||||||
| chr12:125103293
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(182): Show | 188 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.767+212A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103293 | ||||||
| chr12:125103441
|
G | A | 2 | a0001c0001t0001g0079a0002c0002t0001g0075 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.767+360G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103441 | ||||||
| chr12:125103448
|
CACG | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(36): Show | 40 | HG01243.hp1 HG01361.hp1 HG01515.hp2 others(37): Show |
intron_variant | MODIFIER | c.767+370_767+372del others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103448 | |||||
| chr12:125103457
|
G | GCA | 181 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(178): Show | 184 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.767+381_767+382dup others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103457 | |||||
| chr12:125103537
|
GTGTA | G | 86 | a0001c0001t0001g0039a0001c0001t0001g0161a0001c0001t0001g0169others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.767+463_767+466del others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103537 | |||||
| chr12:125103648
|
G | A | 2 | a0002c0007t0001g0017a0002c0007t0001g0027 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.767+567G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103648 | ||||||
| chr12:125103651
|
G | A | 181 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(178): Show | 184 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.767+570G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103651 | ||||||
| chr12:125103784
|
C | T | 22 | a0001c0001t0001g0287a0001c0004t0001g0212a0001c0004t0001g0213others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.767+703C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103784 | ||||||
| chr12:125103805
|
G | A | 4 | a0002c0002t0001g0004a0002c0002t0001g0264a0005c0014t0001g0339others(1): Show | 5 | HG01243.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+724G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103805 | ||||||
| chr12:125103814
|
C | T | 22 | a0001c0001t0001g0287a0001c0004t0001g0212a0001c0004t0001g0213others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.767+733C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103814 | ||||||
| chr12:125103822
|
A | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+741A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103822 | ||||||
| chr12:125103826
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+745G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103826 | ||||||
| chr12:125103845
|
A | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+764A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103845 | ||||||
| chr12:125103848
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+767T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103848 | ||||||
| chr12:125103856
|
C | T | 11 | a0001c0001t0003g0288a0001c0001t0003g0290a0001c0001t0003g0292others(8): Show | 11 | HG01099.hp1 HG01123.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.767+775C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103856 | ||||||
| chr12:125103861
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+780A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103861 | ||||||
| chr12:125103891
|
G | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+810G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103891 | ||||||
| chr12:125103944
|
C | T | 2 | a0001c0001t0001g0079a0002c0002t0001g0075 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.767+863C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125103944 | ||||||
| chr12:125103987
|
C | CA | 40 | a0001c0001t0001g0039a0001c0001t0001g0078a0001c0001t0001g0079others(37): Show | 40 | HG00140.hp2 HG00735.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.767+938dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAA | 44 | a0001c0001t0001g0030a0001c0001t0001g0062a0001c0001t0001g0067others(41): Show | 44 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.767+937_767+938dup others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAAA | 46 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0049others(43): Show | 48 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.767+936_767+938dup others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAAAA | 34 | a0001c0001t0001g0028a0001c0001t0001g0190a0001c0001t0001g0282others(31): Show | 34 | HG00558.hp1 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.767+935_767+938dup others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAAAAA | 35 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0065others(32): Show | 36 | HG00597.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.767+934_767+938dup others(5): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAAAAAA | 26 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0001g0284others(23): Show | 26 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.767+933_767+938dup others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAAAAAAA | 8 | a0001c0001t0001g0275a0001c0001t0001g0289a0001c0001t0001g0319others(5): Show | 8 | HG02145.hp1 HG03669.hp1 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.767+932_767+938dup others(7): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0088 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.767+927_767+938dup others(12): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0087 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.767+926_767+938dup others(13): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.767+921_767+938dup others(18): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CA | C | 9 | a0001c0001t0003g0044a0001c0001t0003g0312a0001c0001t0003g0317others(6): Show | 10 | HG01981.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+938delA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAA | C | 19 | a0001c0001t0001g0035a0001c0001t0001g0077a0001c0001t0001g0340others(16): Show | 19 | HG01243.hp1 HG01243.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.767+937_767+938del others(2): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAAA | C | 15 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0097others(12): Show | 15 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.767+936_767+938del others(3): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAAAAAAA others(3): Show |
C | 11 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+929_767+938del others(10): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0195a0002c0002t0001g0267 | 2 | HG01106.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.767+928_767+938del others(11): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0304 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.767+927_767+938del others(12): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAAAAAAA others(6): Show |
C | 7 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG00733.hp2 HG02922.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.767+926_767+938del others(13): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.767+925_767+938del others(14): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0001g0010a0001c0015t0001g0070a0002c0010t0001g0018 | 3 | HG03139.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.767+922_767+938del others(17): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125103987
|
CAAAAAAA others(12): Show |
C | 22 | a0001c0001t0001g0287a0001c0004t0001g0212a0001c0004t0001g0213others(19): Show | 22 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.767+920_767+938del others(19): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125103987 | |||||
| chr12:125104032
|
T | G | 132 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(129): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.767+951T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104032 | ||||||
| chr12:125104079
|
C | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(30): Show | 34 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.767+998C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104079 | ||||||
| chr12:125104101
|
G | C | 4 | a0001c0003t0001g0053a0001c0003t0001g0354a0001c0003t0001g0355others(1): Show | 4 | HG02258.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+1020G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104101 | ||||||
| chr12:125104174
|
A | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(185): Show | 191 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.767+1093A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104174 | ||||||
| chr12:125104361
|
G | T | 1 | a0001c0003t0001g0353 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.767+1280G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104361 | ||||||
| chr12:125104431
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0231 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.767+1350C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104431 | ||||||
| chr12:125104445
|
A | G | 184 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(181): Show | 187 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.767+1364A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104445 | ||||||
| chr12:125104530
|
G | C | 20 | a0001c0004t0001g0212a0001c0004t0001g0213a0001c0004t0004g0098others(17): Show | 20 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.767+1449G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104530 | ||||||
| chr12:125104593
|
G | C | 1 | a0001c0001t0002g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.767+1512G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104593 | ||||||
| chr12:125104600
|
G | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+1519G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104600 | ||||||
| chr12:125104680
|
G | C | 1 | a0001c0001t0006g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.767+1599G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104680 | ||||||
| chr12:125104849
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.767+1768A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104849 | ||||||
| chr12:125104854
|
A | G | 2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.767+1773A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104854 | ||||||
| chr12:125104860
|
G | A | 2 | a0001c0001t0001g0287a0002c0025t0001g0255 | 2 | HG01175.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.767+1779G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125104860 | ||||||
| chr12:125105020
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.767+1939A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105020 | ||||||
| chr12:125105150
|
C | G | 3 | a0001c0001t0001g0190a0001c0001t0001g0207a0001c0001t0001g0227 | 3 | NA18992.hp2 NA19063.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.768-1971C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105150 | ||||||
| chr12:125105312
|
C | A | 9 | a0001c0004t0004g0167a0001c0004t0004g0237a0001c0004t0004g0242others(6): Show | 9 | HG00597.hp2 HG02015.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-1809C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105312 | ||||||
| chr12:125105392
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.768-1729C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105392 | ||||||
| chr12:125105407
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.768-1714G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105407 | ||||||
| chr12:125105586
|
G | A | 4 | a0002c0002t0001g0004a0002c0002t0001g0264a0005c0014t0001g0339others(1): Show | 5 | HG01243.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-1535G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105586 | ||||||
| chr12:125105603
|
G | T | 1 | a0001c0001t0005g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.768-1518G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105603 | ||||||
| chr12:125105610
|
G | A | 3 | a0001c0001t0001g0159a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG00733.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.768-1511G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105610 | ||||||
| chr12:125105716
|
C | T | 86 | a0001c0001t0001g0039a0001c0001t0001g0161a0001c0001t0001g0169others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.768-1405C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105716 | ||||||
| chr12:125105750
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.768-1371G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105750 | ||||||
| chr12:125105809
|
C | T | 12 | a0001c0003t0001g0053a0001c0003t0001g0354a0001c0003t0001g0355others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.768-1312C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105809 | ||||||
| chr12:125105837
|
A | G | 21 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 22 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.768-1284A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105837 | ||||||
| chr12:125105871
|
T | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(192): Show | 198 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.768-1250T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105871 | ||||||
| chr12:125105888
|
A | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(36): Show | 40 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.768-1233A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105888 | ||||||
| chr12:125105911
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.768-1210G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105911 | ||||||
| chr12:125105912
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.768-1209A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105912 | ||||||
| chr12:125105948
|
T | C | 2 | a0001c0001t0001g0287a0002c0025t0001g0255 | 2 | HG01175.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.768-1173T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125105948 | ||||||
| chr12:125106013
|
G | T | 4 | a0001c0003t0001g0053a0001c0003t0001g0354a0001c0003t0001g0355others(1): Show | 4 | HG02258.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.768-1108G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125106013 | ||||||
| chr12:125106138
|
C | T | 2 | a0002c0007t0001g0017a0002c0007t0001g0027 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.768-983C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125106138 | ||||||
| chr12:125106236
|
T | C | 2 | a0001c0009t0001g0348a0001c0009t0001g0349 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.768-885T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125106236 | ||||||
| chr12:125106406
|
A | G | 57 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0069others(54): Show | 59 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.768-715A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125106406 | ||||||
| chr12:125106680
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.768-441A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125106680 | ||||||
| chr12:125106704
|
C | T | 34 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(31): Show | 34 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.768-417C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125106704 | ||||||
| chr12:125107008
|
A | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0257a0001c0001t0001g0356others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.768-113A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125107008 | ||||||
| chr12:125107023
|
G | A | 13 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(10): Show | 13 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.768-98G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | chr12 | 125107023 | ||||||
| chr12:125107034
|
CAG | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0074others(5): Show | 8 | HG02257.hp2 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.768-84_768-83delAG | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 125107034 | |||||
| chr12:125107298
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(127): Show | 133 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.915+30C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107298 | ||||||
| chr12:125107390
|
G | A | 1 | a0002c0025t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.915+122G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107390 | ||||||
| chr12:125107477
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.915+209G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107477 | ||||||
| chr12:125107522
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0079others(7): Show | 10 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.915+254C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107522 | ||||||
| chr12:125107627
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(181): Show | 187 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.915+359T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107627 | ||||||
| chr12:125107658
|
G | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 6 | HG01109.hp1 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+390G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107658 | ||||||
| chr12:125107686
|
C | T | 4 | a0001c0001t0001g0074a0002c0002t0001g0094a0002c0002t0001g0095others(1): Show | 4 | HG02647.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+418C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107686 | ||||||
| chr12:125107703
|
A | G | 3 | a0001c0001t0005g0103a0001c0001t0005g0104a0002c0002t0001g0011 | 3 | HG02572.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.915+435A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107703 | ||||||
| chr12:125107765
|
C | T | 1 | a0002c0002t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.915+497C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107765 | ||||||
| chr12:125107840
|
G | A | 32 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0162others(29): Show | 32 | HG01243.hp1 HG01361.hp1 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.915+572G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107840 | ||||||
| chr12:125107983
|
T | C | 1 | a0001c0003t0001g0215 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.915+715T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125107983 | ||||||
| chr12:125108002
|
C | T | 5 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(2): Show | 5 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+734C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108002 | ||||||
| chr12:125108048
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.915+780C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108048 | ||||||
| chr12:125108089
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.915+821C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108089 | ||||||
| chr12:125108159
|
A | G | 1 | a0001c0001t0003g0311 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.915+891A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108159 | ||||||
| chr12:125108234
|
G | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(2): Show | 5 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+966G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108234 | ||||||
| chr12:125108357
|
C | T | 1 | a0001c0003t0001g0342 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.915+1089C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108357 | ||||||
| chr12:125108464
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 98 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.915+1196C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108464 | ||||||
| chr12:125108507
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 98 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.915+1239A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108507 | ||||||
| chr12:125108545
|
A | G | 7 | a0001c0001t0001g0077a0001c0001t0001g0356a0001c0001t0001g0357others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+1277A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108545 | ||||||
| chr12:125108570
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.915+1302C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108570 | ||||||
| chr12:125108639
|
G | C | 1 | a0002c0002t0001g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.915+1371G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108639 | ||||||
| chr12:125108675
|
T | A | 7 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107others(4): Show | 7 | HG01515.hp2 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+1407T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108675 | ||||||
| chr12:125108676
|
A | T | 20 | a0001c0001t0001g0257a0001c0001t0005g0103a0001c0001t0005g0104others(17): Show | 20 | HG01243.hp1 HG01361.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+1408A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108676 | ||||||
| chr12:125108772
|
G | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(147): Show | 153 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.915+1504G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108772 | ||||||
| chr12:125108812
|
C | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 140 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.915+1544C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108812 | ||||||
| chr12:125108813
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.915+1545G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108813 | ||||||
| chr12:125108863
|
C | CT | 8 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107others(5): Show | 8 | HG01515.hp2 HG01928.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.915+1612dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125108863 | |||||
| chr12:125108863
|
CT | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.915+1612delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125108863 | |||||
| chr12:125108863
|
CTT | C | 5 | a0001c0001t0002g0176a0002c0002t0001g0004a0002c0002t0001g0264others(2): Show | 6 | HG02698.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+1611_915+1612d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125108863 | |||||
| chr12:125108960
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.915+1692G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125108960 | ||||||
| chr12:125109028
|
C | T | 1 | a0001c0001t0005g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.915+1760C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109028 | ||||||
| chr12:125109037
|
C | A | 37 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(34): Show | 37 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.915+1769C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109037 | ||||||
| chr12:125109125
|
A | G | 15 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0093others(12): Show | 15 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.915+1857A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109125 | ||||||
| chr12:125109234
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0156 | 2 | HG02071.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.915+1966C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109234 | ||||||
| chr12:125109260
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.915+1992T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109260 | ||||||
| chr12:125109435
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 8 | HG02922.hp2 HG03139.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.915+2167C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109435 | ||||||
| chr12:125109522
|
C | T | 1 | a0001c0001t0001g0315 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.915+2254C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109522 | ||||||
| chr12:125109610
|
C | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 140 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.915+2342C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109610 | ||||||
| chr12:125109611
|
G | A | 4 | a0001c0001t0005g0060a0001c0001t0005g0072a0001c0001t0005g0099others(1): Show | 4 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+2343G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109611 | ||||||
| chr12:125109699
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(127): Show | 133 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.915+2431G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109699 | ||||||
| chr12:125109897
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | HG00558.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.915+2629G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125109897 | ||||||
| chr12:125110024
|
C | CT | 137 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 140 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.915+2768dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110024 | |||||
| chr12:125110170
|
C | T | 7 | a0001c0001t0001g0085a0001c0001t0006g0186a0001c0001t0006g0197others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+2902C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125110170 | ||||||
| chr12:125110188
|
TTTGTGTG | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0228a0002c0002t0001g0118 | 3 | HG03491.hp1 HG03540.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.915+2922_915+2928d others(9): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110188 | |||||
| chr12:125110188
|
TTTGTGTG others(10): Show |
T | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.915+2922_915+2938d others(19): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110188 | |||||
| chr12:125110188
|
TTTGTGTG others(12): Show |
T | 1 | a0001c0004t0004g0243 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.915+2922_915+2940d others(21): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110188 | |||||
| chr12:125110189
|
TTGTG | T | 7 | a0001c0001t0001g0283a0001c0001t0001g0319a0001c0001t0011g0108others(4): Show | 7 | HG01071.hp1 HG01891.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+2979_915+2982d others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTG | T | 16 | a0001c0001t0001g0172a0001c0001t0001g0258a0001c0001t0001g0282others(13): Show | 16 | HG00558.hp1 HG00642.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.915+2977_915+2982d others(8): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(1): Show |
T | 40 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0001g0088others(37): Show | 40 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.915+2975_915+2982d others(10): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(3): Show |
T | 75 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0061others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.915+2973_915+2982d others(12): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(5): Show |
T | 37 | a0001c0001t0001g0038a0001c0001t0001g0062a0001c0001t0001g0066others(34): Show | 37 | HG00735.hp2 HG01099.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.915+2971_915+2982d others(14): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(7): Show |
T | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0031others(25): Show | 28 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.915+2969_915+2982d others(16): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(9): Show |
T | 18 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(15): Show | 18 | HG00544.hp2 HG01074.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.915+2967_915+2982d others(18): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(11): Show |
T | 13 | a0001c0001t0005g0072a0001c0001t0005g0103a0001c0001t0005g0104others(10): Show | 13 | HG00597.hp2 HG02040.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.915+2965_915+2982d others(20): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(13): Show |
T | 8 | a0001c0001t0001g0287a0001c0001t0002g0188a0001c0001t0002g0201others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+2963_915+2982d others(22): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(15): Show |
T | 6 | a0001c0001t0001g0159a0001c0001t0001g0203a0001c0001t0002g0200others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+2961_915+2982d others(24): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(17): Show |
T | 7 | a0001c0001t0001g0054a0001c0001t0001g0251a0001c0001t0002g0155others(4): Show | 8 | HG02615.hp1 HG02723.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.915+2959_915+2982d others(26): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(19): Show |
T | 87 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(84): Show | 89 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.915+2957_915+2982d others(28): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110189
|
TTGTGTGT others(21): Show |
T | 1 | a0001c0001t0005g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.915+2955_915+2982d others(30): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110189 | |||||
| chr12:125110231
|
GTGTGTGT others(12): Show |
G | 1 | a0001c0004t0004g0245 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.915+2965_915+2983d others(21): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110231 | |||||
| chr12:125110237
|
GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0352 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.915+2971_915+2983d others(15): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125110237 | |||||
| chr12:125110340
|
G | A | 1 | a0001c0003t0001g0225 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.915+3072G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125110340 | ||||||
| chr12:125110375
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0001g0300a0001c0001t0001g0345 | 3 | NA18943.hp2 NA18952.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.915+3107G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125110375 | ||||||
| chr12:125110512
|
G | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(126): Show | 132 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.915+3244G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125110512 | ||||||
| chr12:125110534
|
C | T | 1 | a0002c0002t0005g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.915+3266C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125110534 | ||||||
| chr12:125111029
|
C | G | 1 | a0001c0004t0001g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.916-3448C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111029 | ||||||
| chr12:125111044
|
G | C | 2 | a0002c0002t0001g0094a0002c0002t0001g0095 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.916-3433G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111044 | ||||||
| chr12:125111105
|
C | T | 2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.916-3372C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111105 | ||||||
| chr12:125111210
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.916-3267C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111210 | ||||||
| chr12:125111297
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.916-3180A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111297 | ||||||
| chr12:125111303
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0306a0001c0001t0001g0352 | 3 | NA18986.hp2 NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.916-3174G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111303 | ||||||
| chr12:125111307
|
C | T | 1 | a0001c0001t0005g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.916-3170C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111307 | ||||||
| chr12:125111386
|
T | C | 1 | a0001c0003t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.916-3091T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111386 | ||||||
| chr12:125111587
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.916-2890T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111587 | ||||||
| chr12:125111794
|
C | T | 1 | a0002c0002t0001g0127 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.916-2683C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111794 | ||||||
| chr12:125111830
|
A | G | 7 | a0001c0001t0001g0340a0002c0005t0001g0015a0002c0005t0001g0020others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-2647A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111830 | ||||||
| chr12:125111842
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.916-2635G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111842 | ||||||
| chr12:125111883
|
C | T | 1 | a0002c0002t0001g0131 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.916-2594C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111883 | ||||||
| chr12:125111901
|
AGAG | A | 13 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(10): Show | 13 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.916-2568_916-2566d others(5): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125111901 | |||||
| chr12:125111912
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 98 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.916-2565G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111912 | ||||||
| chr12:125111958
|
C | T | 3 | a0001c0001t0005g0103a0001c0001t0005g0104a0002c0002t0001g0011 | 3 | HG02572.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.916-2519C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111958 | ||||||
| chr12:125111966
|
G | A | 3 | a0001c0001t0005g0103a0001c0001t0005g0104a0002c0002t0001g0011 | 3 | HG02572.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.916-2511G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125111966 | ||||||
| chr12:125112205
|
T | C | 1 | a0001c0001t0003g0330 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.916-2272T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125112205 | ||||||
| chr12:125112322
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-2155C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125112322 | ||||||
| chr12:125112530
|
A | G | 1 | a0001c0001t0002g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.916-1947A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125112530 | ||||||
| chr12:125112638
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.916-1839C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125112638 | ||||||
| chr12:125112678
|
C | CA | 6 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02257.hp1 HG03239.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-1786dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125112678 | |||||
| chr12:125112678
|
C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0077a0001c0001t0001g0356a0001c0001t0001g0357others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.916-1794_916-1786d others(11): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125112678 | |||||
| chr12:125112678
|
C | CAAAAAAA others(3): Show |
32 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(29): Show | 32 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.916-1795_916-1786d others(12): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125112678 | |||||
| chr12:125112678
|
C | CAAAAAAA others(4): Show |
111 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(108): Show | 114 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.916-1796_916-1786d others(13): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125112678 | |||||
| chr12:125112678
|
C | CAAAAAAA others(5): Show |
29 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0091others(26): Show | 29 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.916-1797_916-1786d others(14): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125112678 | |||||
| chr12:125112678
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0002g0187a0009c0024t0001g0263 | 2 | HG03688.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.916-1798_916-1786d others(15): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 125112678 | |||||
| chr12:125112845
|
A | T | 7 | a0001c0001t0001g0077a0001c0001t0001g0356a0001c0001t0001g0357others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-1632A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125112845 | ||||||
| chr12:125112898
|
C | G | 4 | a0002c0002t0001g0004a0002c0002t0001g0264a0005c0014t0001g0339others(1): Show | 5 | HG01243.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-1579C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125112898 | ||||||
| chr12:125112931
|
C | T | 2 | a0002c0002t0001g0273a0002c0002t0001g0274 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.916-1546C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125112931 | ||||||
| chr12:125112932
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.916-1545G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125112932 | ||||||
| chr12:125113129
|
G | A | 2 | a0001c0015t0001g0070a0002c0010t0001g0018 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.916-1348G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113129 | ||||||
| chr12:125113306
|
C | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(3): Show | 6 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.916-1171C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113306 | ||||||
| chr12:125113395
|
G | A | 2 | a0001c0001t0001g0287a0002c0025t0001g0255 | 2 | HG01175.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.916-1082G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113395 | ||||||
| chr12:125113623
|
G | A | 4 | a0002c0002t0001g0004a0002c0002t0001g0264a0005c0014t0001g0339others(1): Show | 5 | HG01243.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-854G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113623 | ||||||
| chr12:125113693
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02922.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-784A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113693 | ||||||
| chr12:125113741
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.916-736C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113741 | ||||||
| chr12:125113843
|
C | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 17 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.916-634C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113843 | ||||||
| chr12:125113910
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-567C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113910 | ||||||
| chr12:125113992
|
C | T | 1 | a0005c0014t0001g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.916-485C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125113992 | ||||||
| chr12:125114058
|
G | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(128): Show | 134 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.916-419G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125114058 | ||||||
| chr12:125114068
|
G | A | 7 | a0001c0001t0001g0340a0002c0005t0001g0015a0002c0005t0001g0020others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-409G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125114068 | ||||||
| chr12:125114185
|
G | T | 1 | a0002c0002t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.916-292G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125114185 | ||||||
| chr12:125114266
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.916-211C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125114266 | ||||||
| chr12:125114291
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.916-186A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125114291 | ||||||
| chr12:125114382
|
C | G | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.916-95C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125114382 | ||||||
| chr12:125114402
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.916-75G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 8/17 | chr12 | 125114402 | ||||||
| chr12:125114574
|
G | A | 1 | a0002c0021t0001g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.996+17G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114574 | ||||||
| chr12:125114588
|
T | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 17 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.996+31T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114588 | ||||||
| chr12:125114594
|
A | G | 1 | a0001c0001t0005g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.996+37A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114594 | ||||||
| chr12:125114639
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(28): Show | 32 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.996+82A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114639 | ||||||
| chr12:125114654
|
G | A | 3 | a0001c0001t0002g0057a0001c0001t0002g0073a0001c0001t0002g0187 | 3 | HG02683.hp2 HG03209.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.996+97G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114654 | ||||||
| chr12:125114662
|
GCACATGG others(68): Show |
G | 87 | a0001c0001t0001g0039a0001c0001t0001g0161a0001c0001t0001g0169others(84): Show | 88 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.996+129_996+203del others(75): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125114662 | |||||
| chr12:125114685
|
G | GTGCTGGC others(104): Show |
1 | a0002c0002t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.996+238_996+239ins others(111): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125114685 | |||||
| chr12:125114765
|
G | A | 1 | a0001c0001t0006g0197 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.996+208G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114765 | ||||||
| chr12:125114794
|
A | AGGCGCCG others(29): Show |
3 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0009 | 3 | HG02145.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.996+315_996+350dup others(36): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125114794 | |||||
| chr12:125114794
|
AGGCGCCG others(29): Show |
A | 2 | a0001c0001t0001g0109a0002c0002t0001g0075 | 2 | HG01099.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.996+315_996+350del others(36): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125114794 | |||||
| chr12:125114809
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.996+252G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114809 | ||||||
| chr12:125114866
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0093others(15): Show | 18 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.996+309G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114866 | ||||||
| chr12:125114877
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02922.hp2 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.996+320C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114877 | ||||||
| chr12:125114881
|
GCACATGG others(29): Show |
G | 1 | a0001c0001t0003g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.996+351_996+386del others(36): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125114881 | |||||
| chr12:125114941
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.996+384C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114941 | ||||||
| chr12:125114963
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.996+406G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125114963 | ||||||
| chr12:125115016
|
A | G | 2 | a0001c0015t0001g0070a0002c0010t0001g0018 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.996+459A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115016 | ||||||
| chr12:125115029
|
G | A | 7 | a0001c0001t0001g0077a0001c0001t0001g0356a0001c0001t0001g0357others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.996+472G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115029 | ||||||
| chr12:125115043
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.996+486C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115043 | ||||||
| chr12:125115247
|
G | A | 1 | a0002c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.996+690G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115247 | ||||||
| chr12:125115260
|
G | GT | 32 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(29): Show | 32 | HG01175.hp1 HG01175.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.996+721dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125115260 | |||||
| chr12:125115260
|
GT | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0039a0001c0001t0001g0162others(7): Show | 10 | HG01168.hp2 HG02922.hp2 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+721delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125115260 | |||||
| chr12:125115301
|
C | G | 2 | a0001c0015t0001g0070a0002c0010t0001g0018 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.996+744C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115301 | ||||||
| chr12:125115682
|
C | T | 1 | a0002c0002t0001g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.996+1125C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115682 | ||||||
| chr12:125115685
|
C | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.996+1128C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115685 | ||||||
| chr12:125115784
|
G | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02922.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.996+1227G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115784 | ||||||
| chr12:125115898
|
C | T | 1 | a0002c0002t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.996+1341C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115898 | ||||||
| chr12:125115976
|
C | T | 1 | a0001c0001t0006g0186 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.996+1419C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115976 | ||||||
| chr12:125115998
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.996+1441T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125115998 | ||||||
| chr12:125116017
|
AT | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02922.hp2 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.996+1462delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125116017 | |||||
| chr12:125116033
|
A | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0162others(4): Show | 7 | HG02486.hp1 HG02922.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.996+1476A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116033 | ||||||
| chr12:125116159
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02922.hp2 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.996+1602T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116159 | ||||||
| chr12:125116178
|
G | A | 20 | a0001c0001t0001g0097a0001c0001t0001g0257a0001c0001t0005g0105others(17): Show | 20 | HG01243.hp1 HG01361.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.996+1621G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116178 | ||||||
| chr12:125116390
|
C | T | 1 | a0001c0001t0010g0194 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.996+1833C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116390 | ||||||
| chr12:125116431
|
G | T | 2 | a0001c0001t0002g0252a0001c0017t0002g0204 | 2 | NA18957.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.996+1874G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116431 | ||||||
| chr12:125116493
|
T | C | 2 | a0001c0001t0002g0071a0001c0001t0002g0082 | 2 | HG02165.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.996+1936T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116493 | ||||||
| chr12:125116530
|
T | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(135): Show | 141 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.996+1973T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116530 | ||||||
| chr12:125116620
|
C | A | 1 | a0001c0001t0001g0307 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.997-2021C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116620 | ||||||
| chr12:125116620
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.997-2021C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116620 | ||||||
| chr12:125116768
|
C | T | 2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.997-1873C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116768 | ||||||
| chr12:125116950
|
C | T | 1 | a0002c0007t0001g0016 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.997-1691C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125116950 | ||||||
| chr12:125117147
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0337 | 2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.997-1494C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125117147 | ||||||
| chr12:125117413
|
C | CA | 18 | a0001c0001t0001g0028a0001c0001t0001g0091a0001c0001t0001g0093others(15): Show | 18 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.997-1214dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125117413 | |||||
| chr12:125117454
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.997-1187C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125117454 | ||||||
| chr12:125117523
|
A | G | 357 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(354): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.997-1118A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125117523 | ||||||
| chr12:125117592
|
A | G | 1 | a0001c0001t0005g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.997-1049A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125117592 | ||||||
| chr12:125117668
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.997-973C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125117668 | ||||||
| chr12:125117686
|
TTCAGAAA others(5): Show |
T | 1 | a0001c0001t0002g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.997-951_997-940del others(12): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125117686 | |||||
| chr12:125117714
|
G | A | 1 | a0001c0001t0006g0336 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.997-927G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125117714 | ||||||
| chr12:125117727
|
T | C | 1 | a0002c0005t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.997-914T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125117727 | ||||||
| chr12:125117791
|
G | A | 1 | a0001c0001t0002g0347 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.997-850G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125117791 | ||||||
| chr12:125117988
|
G | GA | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(135): Show | 141 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.997-640dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 125117988 | |||||
| chr12:125118009
|
G | A | 8 | a0001c0001t0001g0172a0002c0002t0001g0102a0002c0002t0001g0117others(5): Show | 8 | NA18939.hp2 NA18944.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.997-632G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125118009 | ||||||
| chr12:125118138
|
T | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(135): Show | 141 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.997-503T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125118138 | ||||||
| chr12:125118171
|
C | A | 1 | a0001c0001t0001g0333 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.997-470C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125118171 | ||||||
| chr12:125118216
|
G | A | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0301 | 3 | NA18950.hp2 NA19007.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.997-425G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125118216 | ||||||
| chr12:125118430
|
A | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0091others(17): Show | 20 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.997-211A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125118430 | ||||||
| chr12:125118606
|
C | T | 51 | a0001c0001t0001g0029a0001c0001t0001g0061a0001c0001t0001g0065others(48): Show | 51 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.997-35C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125118606 | ||||||
| chr12:125118625
|
C | T | 1 | a0004c0018t0003g0280 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.997-16C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 9/17 | chr12 | 125118625 | ||||||
| chr12:125118820
|
C | T | 1 | a0002c0002t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1121+55C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125118820 | ||||||
| chr12:125118897
|
G | A | 1 | a0002c0007t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1121+132G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125118897 | ||||||
| chr12:125119096
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1121+331G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119096 | ||||||
| chr12:125119253
|
A | G | 3 | a0001c0003t0001g0053a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1121+488A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119253 | ||||||
| chr12:125119265
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1121+500G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119265 | ||||||
| chr12:125119394
|
G | A | 12 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(9): Show | 12 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121+629G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119394 | ||||||
| chr12:125119402
|
G | T | 12 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(9): Show | 12 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121+637G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119402 | ||||||
| chr12:125119631
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1121+866C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119631 | ||||||
| chr12:125119788
|
C | T | 1 | a0001c0001t0003g0310 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1121+1023C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119788 | ||||||
| chr12:125119886
|
G | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0304a0001c0001t0001g0351 | 3 | HG00099.hp2 HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1121+1121G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119886 | ||||||
| chr12:125119925
|
C | T | 1 | a0002c0005t0001g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1121+1160C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119925 | ||||||
| chr12:125119986
|
C | A | 2 | a0001c0001t0001g0287a0002c0025t0001g0255 | 2 | HG01175.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1121+1221C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125119986 | ||||||
| chr12:125120072
|
C | T | 1 | a0001c0001t0002g0297 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1121+1307C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120072 | ||||||
| chr12:125120147
|
C | A | 1 | a0001c0003t0001g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1121+1382C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120147 | ||||||
| chr12:125120267
|
G | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1121+1502G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120267 | ||||||
| chr12:125120348
|
G | C | 1 | a0001c0001t0001g0319 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1121+1583G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120348 | ||||||
| chr12:125120416
|
G | C | 2 | a0001c0015t0001g0070a0002c0010t0001g0018 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1121+1651G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120416 | ||||||
| chr12:125120528
|
G | A | 1 | a0002c0002t0001g0135 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1121+1763G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120528 | ||||||
| chr12:125120667
|
G | A | 1 | a0002c0002t0005g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1121+1902G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120667 | ||||||
| chr12:125120698
|
G | T | 1 | a0001c0001t0006g0084 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1121+1933G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120698 | ||||||
| chr12:125120743
|
G | T | 3 | a0001c0003t0001g0053a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1121+1978G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120743 | ||||||
| chr12:125120786
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1121+2021T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120786 | ||||||
| chr12:125120910
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0159 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1121+2145A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120910 | ||||||
| chr12:125120962
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1121+2197A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125120962 | ||||||
| chr12:125121018
|
T | A | 6 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(3): Show | 6 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+2253T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121018 | ||||||
| chr12:125121108
|
C | T | 1 | a0002c0002t0001g0129 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1121+2343C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121108 | ||||||
| chr12:125121177
|
C | T | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0054others(2): Show | 5 | HG02559.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+2412C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121177 | ||||||
| chr12:125121228
|
C | A | 1 | a0002c0005t0001g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1121+2463C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121228 | ||||||
| chr12:125121245
|
T | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(28): Show | 33 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.1121+2480T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121245 | ||||||
| chr12:125121285
|
G | A | 2 | a0001c0001t0001g0287a0002c0025t0001g0255 | 2 | HG01175.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1121+2520G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121285 | ||||||
| chr12:125121325
|
C | T | 2 | a0002c0002t0007g0112a0002c0002t0007g0113 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1121+2560C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121325 | ||||||
| chr12:125121331
|
C | T | 1 | a0001c0001t0005g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1121+2566C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121331 | ||||||
| chr12:125121341
|
A | G | 89 | a0001c0001t0001g0039a0001c0001t0001g0161a0001c0001t0001g0169others(86): Show | 90 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1121+2576A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121341 | ||||||
| chr12:125121400
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(40): Show | 45 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.1121+2635C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121400 | ||||||
| chr12:125121411
|
C | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(134): Show | 140 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1121+2646C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121411 | ||||||
| chr12:125121577
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(135): Show | 141 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1121+2812G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121577 | ||||||
| chr12:125121634
|
C | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(135): Show | 141 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1121+2869C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121634 | ||||||
| chr12:125121678
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1121+2913T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121678 | ||||||
| chr12:125121839
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1122-2866C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121839 | ||||||
| chr12:125121857
|
A | G | 7 | a0001c0001t0001g0077a0001c0001t0001g0356a0001c0001t0001g0357others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-2848A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121857 | ||||||
| chr12:125121858
|
C | T | 1 | a0002c0021t0001g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1122-2847C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121858 | ||||||
| chr12:125121881
|
G | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(181): Show | 187 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.1122-2824G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121881 | ||||||
| chr12:125121882
|
G | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(181): Show | 187 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.1122-2823G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125121882 | ||||||
| chr12:125122040
|
CGAGAGGT others(3): Show |
C | 1 | a0001c0001t0002g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1122-2663_1122-265 others(14): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 125122040 | |||||
| chr12:125122104
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02922.hp2 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-2601C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122104 | ||||||
| chr12:125122217
|
G | A | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG00642.hp1 HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1122-2488G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122217 | ||||||
| chr12:125122223
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1122-2482G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122223 | ||||||
| chr12:125122278
|
C | T | 13 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(10): Show | 13 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122-2427C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122278 | ||||||
| chr12:125122580
|
T | C | 3 | a0001c0003t0001g0053a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02258.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1122-2125T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122580 | ||||||
| chr12:125122642
|
C | CA | 130 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(127): Show | 133 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1122-2045dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 125122642 | |||||
| chr12:125122642
|
C | CAA | 17 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0093others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1122-2046_1122-204 others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 125122642 | |||||
| chr12:125122791
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0337 | 2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1122-1914C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122791 | ||||||
| chr12:125122838
|
C | T | 12 | a0001c0001t0001g0097a0001c0001t0001g0257a0001c0001t0001g0285others(9): Show | 12 | HG00099.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1122-1867C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122838 | ||||||
| chr12:125122848
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02922.hp2 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-1857A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122848 | ||||||
| chr12:125122934
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1122-1771C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125122934 | ||||||
| chr12:125123057
|
A | G | 24 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(21): Show | 24 | HG00544.hp2 HG00597.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.1122-1648A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123057 | ||||||
| chr12:125123081
|
T | C | 357 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(354): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1122-1624T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123081 | ||||||
| chr12:125123083
|
C | T | 5 | a0001c0001t0001g0327a0002c0002t0001g0121a0002c0002t0001g0130others(2): Show | 5 | HG00621.hp2 NA18964.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122-1622C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123083 | ||||||
| chr12:125123278
|
CAT | C | 3 | a0001c0001t0002g0183a0001c0001t0002g0252a0001c0017t0002g0204 | 3 | NA18953.hp1 NA18957.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1122-1426_1122-142 others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123278 | ||||||
| chr12:125123281
|
T | G | 3 | a0001c0001t0002g0183a0001c0001t0002g0252a0001c0017t0002g0204 | 3 | NA18953.hp1 NA18957.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1122-1424T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123281 | ||||||
| chr12:125123282
|
A | G | 3 | a0001c0001t0002g0183a0001c0001t0002g0252a0001c0017t0002g0204 | 3 | NA18953.hp1 NA18957.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1122-1423A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123282 | ||||||
| chr12:125123482
|
T | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(187): Show | 193 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.1122-1223T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123482 | ||||||
| chr12:125123483
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02922.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1122-1222G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123483 | ||||||
| chr12:125123609
|
G | A | 2 | a0001c0001t0001g0287a0002c0025t0001g0255 | 2 | HG01175.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1122-1096G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123609 | ||||||
| chr12:125123791
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1122-914C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123791 | ||||||
| chr12:125123806
|
G | A | 2 | a0001c0015t0001g0070a0002c0010t0001g0018 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1122-899G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123806 | ||||||
| chr12:125123946
|
T | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(137): Show | 143 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1122-759T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125123946 | ||||||
| chr12:125124043
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1122-662C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125124043 | ||||||
| chr12:125124249
|
T | G | 9 | a0001c0001t0001g0327a0002c0002t0001g0121a0002c0002t0001g0130others(6): Show | 9 | HG00621.hp2 NA18954.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.1122-456T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125124249 | ||||||
| chr12:125124437
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1122-268C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125124437 | ||||||
| chr12:125124445
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1122-260C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125124445 | ||||||
| chr12:125124699
|
C | T | 1 | a0001c0001t0003g0219 | 1 | HG00735.hp2 | splice_region_variant&intron_variant | LOW | c.1122-6C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 10/17 | chr12 | 125124699 | ||||||
| chr12:125124838
|
T | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0207a0001c0001t0001g0227others(2): Show | 5 | NA18959.hp2 NA18992.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.1187-64T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 11/17 | chr12 | 125124838 | ||||||
| chr12:125125035
|
G | A | 1 | a0001c0004t0004g0328 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1309+11G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125035 | ||||||
| chr12:125125141
|
G | A | 1 | a0002c0002t0001g0006 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1309+117G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125141 | ||||||
| chr12:125125198
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0333 | 3 | HG00558.hp1 NA18955.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1309+174G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125198 | ||||||
| chr12:125125427
|
C | T | 28 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(25): Show | 28 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1309+403C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125427 | ||||||
| chr12:125125616
|
C | T | 1 | a0001c0001t0002g0321 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1309+592C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125616 | ||||||
| chr12:125125684
|
A | T | 1 | a0002c0002t0001g0121 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1309+660A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125684 | ||||||
| chr12:125125713
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1309+689C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125713 | ||||||
| chr12:125125764
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1309+740C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125764 | ||||||
| chr12:125125807
|
ATGGCCAT | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(155): Show | 161 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.1309+791_1309+797d others(9): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 125125807 | |||||
| chr12:125125841
|
T | C | 2 | a0001c0015t0001g0070a0002c0010t0001g0018 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1309+817T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125125841 | ||||||
| chr12:125125957
|
A | AT | 8 | a0001c0001t0001g0284a0001c0001t0001g0305a0001c0001t0005g0060others(5): Show | 8 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309+950dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 125125957 | |||||
| chr12:125125957
|
AT | A | 139 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(136): Show | 140 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1309+950delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 125125957 | |||||
| chr12:125126049
|
C | T | 1 | a0002c0005t0001g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1309+1025C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126049 | ||||||
| chr12:125126115
|
G | A | 1 | a0001c0003t0001g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1309+1091G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126115 | ||||||
| chr12:125126219
|
C | T | 22 | a0001c0001t0003g0041a0001c0001t0003g0044a0001c0001t0003g0179others(19): Show | 22 | HG01099.hp1 HG01123.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.1309+1195C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126219 | ||||||
| chr12:125126235
|
C | T | 1 | a0001c0001t0003g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1309+1211C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126235 | ||||||
| chr12:125126471
|
C | T | 2 | a0001c0001t0001g0287a0002c0025t0001g0255 | 2 | HG01175.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1309+1447C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126471 | ||||||
| chr12:125126562
|
T | C | 1 | a0001c0001t0002g0322 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1309+1538T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126562 | ||||||
| chr12:125126579
|
G | GT | 134 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 137 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1310-1565dupT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 125126579 | |||||
| chr12:125126725
|
G | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(144): Show | 150 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.1310-1436G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126725 | ||||||
| chr12:125126738
|
C | T | 33 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(30): Show | 33 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1310-1423C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126738 | ||||||
| chr12:125126869
|
C | CAGGCA | 6 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0009others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-1291_1310-129 others(9): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 125126869 | |||||
| chr12:125126871
|
C | A | 6 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0009others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-1290C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126871 | ||||||
| chr12:125126872
|
C | A | 6 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0009others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-1289C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126872 | ||||||
| chr12:125126877
|
C | T | 5 | a0001c0004t0004g0237a0001c0004t0004g0242a0001c0004t0004g0243others(2): Show | 5 | NA18955.hp1 NA18977.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.1310-1284C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125126877 | ||||||
| chr12:125127001
|
A | G | 3 | a0001c0001t0005g0060a0001c0001t0005g0072a0001c0001t0005g0099 | 3 | HG02630.hp1 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1310-1160A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125127001 | ||||||
| chr12:125127140
|
A | T | 1 | a0001c0001t0001g0233 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1310-1021A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125127140 | ||||||
| chr12:125127177
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1310-984C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125127177 | ||||||
| chr12:125127223
|
G | A | 1 | a0001c0003t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1310-938G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125127223 | ||||||
| chr12:125127276
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1310-885A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125127276 | ||||||
| chr12:125127341
|
G | C | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1310-820G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125127341 | ||||||
| chr12:125127551
|
T | G | 4 | a0001c0001t0001g0079a0002c0007t0001g0016a0002c0007t0001g0017others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1310-610T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125127551 | ||||||
| chr12:125127952
|
A | G | 1 | a0001c0003t0001g0214 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1310-209A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125127952 | ||||||
| chr12:125128054
|
A | C | 12 | a0001c0001t0001g0097a0001c0001t0001g0257a0002c0002t0001g0006others(9): Show | 12 | HG01243.hp1 HG01361.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1310-107A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125128054 | ||||||
| chr12:125128071
|
T | C | 1 | a0001c0004t0004g0249 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1310-90T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125128071 | ||||||
| chr12:125128124
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1310-37T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 12/17 | chr12 | 125128124 | ||||||
| chr12:125128293
|
G | A | 119 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(116): Show | 120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1423+19G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128293 | ||||||
| chr12:125128344
|
G | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.1423+70G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128344 | ||||||
| chr12:125128380
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1423+106T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128380 | ||||||
| chr12:125128446
|
C | T | 27 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.1423+172C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128446 | ||||||
| chr12:125128525
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02922.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1423+251G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128525 | ||||||
| chr12:125128604
|
A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0162others(16): Show | 19 | HG01175.hp2 HG01243.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1423+330A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128604 | ||||||
| chr12:125128612
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 16 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1423+338A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128612 | ||||||
| chr12:125128693
|
C | A | 1 | a0001c0001t0002g0156 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1423+419C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128693 | ||||||
| chr12:125128745
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1423+471C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128745 | ||||||
| chr12:125128883
|
C | A | 1 | a0007c0016t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1424-452C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128883 | ||||||
| chr12:125128953
|
C | G | 20 | a0001c0003t0001g0168a0001c0003t0001g0210a0001c0003t0001g0214others(17): Show | 20 | HG00597.hp1 HG00621.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1424-382C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125128953 | ||||||
| chr12:125129009
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG03239.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1424-326A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125129009 | ||||||
| chr12:125129144
|
G | A | 1 | a0001c0001t0006g0198 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1424-191G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125129144 | ||||||
| chr12:125129174
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1424-161T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125129174 | ||||||
| chr12:125129202
|
C | T | 7 | a0001c0001t0001g0077a0001c0001t0001g0356a0001c0001t0001g0357others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1424-133C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125129202 | ||||||
| chr12:125129208
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1424-127C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125129208 | ||||||
| chr12:125129261
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1424-74A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 13/17 | chr12 | 125129261 | ||||||
| chr12:125129579
|
C | T | 32 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1549+119C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125129579 | ||||||
| chr12:125129657
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02922.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1549+197G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125129657 | ||||||
| chr12:125129813
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1549+353C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125129813 | ||||||
| chr12:125129846
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1549+386G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125129846 | ||||||
| chr12:125129915
|
C | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0187 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1549+455C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125129915 | ||||||
| chr12:125130068
|
C | G | 1 | a0005c0014t0001g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1549+608C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125130068 | ||||||
| chr12:125130068
|
C | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0162others(13): Show | 16 | HG01243.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1549+608C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125130068 | ||||||
| chr12:125130250
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1549+790G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125130250 | ||||||
| chr12:125130477
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1549+1017G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125130477 | ||||||
| chr12:125130555
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1549+1095T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125130555 | ||||||
| chr12:125130668
|
T | C | 2 | a0001c0001t0002g0185a0001c0001t0002g0202 | 2 | NA18954.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1549+1208T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125130668 | ||||||
| chr12:125130698
|
C | T | 10 | a0001c0001t0005g0063a0001c0001t0006g0064a0001c0001t0006g0076others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1549+1238C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125130698 | ||||||
| chr12:125131028
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1549+1568C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131028 | ||||||
| chr12:125131051
|
G | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(31): Show | 36 | HG01243.hp1 HG01243.hp2 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.1549+1591G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131051 | ||||||
| chr12:125131063
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 16 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1549+1603C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131063 | ||||||
| chr12:125131064
|
G | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0162others(13): Show | 16 | HG01243.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1549+1604G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131064 | ||||||
| chr12:125131080
|
C | T | 7 | a0001c0001t0001g0340a0002c0005t0001g0015a0002c0005t0001g0020others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1549+1620C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131080 | ||||||
| chr12:125131081
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0097others(17): Show | 20 | HG01243.hp1 HG01361.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1549+1621G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131081 | ||||||
| chr12:125131429
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0158 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1549+1969C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131429 | ||||||
| chr12:125131468
|
T | C | 2 | a0002c0010t0001g0018a0002c0025t0001g0255 | 2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1549+2008T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131468 | ||||||
| chr12:125131566
|
A | G | 2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1549+2106A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131566 | ||||||
| chr12:125131580
|
T | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(34): Show | 39 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1549+2120T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131580 | ||||||
| chr12:125131695
|
G | A | 1 | a0001c0003t0001g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1549+2235G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131695 | ||||||
| chr12:125131745
|
C | T | 109 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0061others(106): Show | 110 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1550-2258C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131745 | ||||||
| chr12:125131746
|
G | A | 4 | a0001c0001t0001g0079a0002c0007t0001g0016a0002c0007t0001g0017others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1550-2257G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131746 | ||||||
| chr12:125131787
|
C | T | 35 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(32): Show | 35 | HG00597.hp2 HG00733.hp2 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.1550-2216C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131787 | ||||||
| chr12:125131788
|
G | A | 1 | a0002c0002t0006g0136 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1550-2215G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131788 | ||||||
| chr12:125131836
|
A | G | 27 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.1550-2167A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131836 | ||||||
| chr12:125131883
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1550-2120C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131883 | ||||||
| chr12:125131889
|
G | C | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1550-2114G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125131889 | ||||||
| chr12:125132037
|
G | A | 25 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(22): Show | 25 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1550-1966G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125132037 | ||||||
| chr12:125132240
|
C | CAG | 23 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0097others(20): Show | 23 | HG01175.hp2 HG01243.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.1550-1763_1550-176 others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125132240 | ||||||
| chr12:125132266
|
C | T | 2 | a0001c0001t0002g0252a0001c0017t0002g0204 | 2 | NA18957.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1550-1737C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125132266 | ||||||
| chr12:125132351
|
A | C | 7 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107others(4): Show | 7 | HG01515.hp2 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1550-1652A>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125132351 | ||||||
| chr12:125132444
|
G | A | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1550-1559G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125132444 | ||||||
| chr12:125132491
|
C | T | 1 | a0001c0004t0001g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1550-1512C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125132491 | ||||||
| chr12:125133178
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02922.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1550-825A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125133178 | ||||||
| chr12:125133191
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1550-812C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125133191 | ||||||
| chr12:125133352
|
C | T | 1 | a0002c0005t0001g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1550-651C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125133352 | ||||||
| chr12:125133371
|
T | G | 21 | a0001c0001t0001g0010a0001c0001t0001g0078a0001c0001t0001g0079others(18): Show | 21 | HG01109.hp1 HG01243.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1550-632T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125133371 | ||||||
| chr12:125133434
|
G | C | 7 | a0001c0001t0005g0060a0001c0001t0005g0072a0001c0001t0005g0099others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1550-569G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125133434 | ||||||
| chr12:125133863
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1550-140C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125133863 | ||||||
| chr12:125133979
|
C | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 9 | HG02145.hp1 HG02145.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1550-24C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 14/17 | chr12 | 125133979 | ||||||
| chr12:125134186
|
C | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0306a0001c0001t0001g0352 | 3 | NA18986.hp2 NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1619+114C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 15/17 | chr12 | 125134186 | ||||||
| chr12:125134198
|
A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0078a0001c0001t0001g0097others(12): Show | 16 | HG01109.hp1 HG01243.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1619+126A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 15/17 | chr12 | 125134198 | ||||||
| chr12:125134300
|
C | G | 3 | a0001c0015t0001g0070a0002c0010t0001g0018a0002c0025t0001g0255 | 3 | HG01175.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1619+228C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 15/17 | chr12 | 125134300 | ||||||
| chr12:125134407
|
C | G | 191 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0033others(188): Show | 192 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.1619+335C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 15/17 | chr12 | 125134407 | ||||||
| chr12:125134613
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1620-181G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 15/17 | chr12 | 125134613 | ||||||
| chr12:125134758
|
G | T | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1620-36G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 15/17 | chr12 | 125134758 | ||||||
| chr12:125134762
|
C | T | 183 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0033others(180): Show | 184 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.1620-32C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 15/17 | chr12 | 125134762 | ||||||
| chr12:125135098
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1678+246G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135098 | ||||||
| chr12:125135128
|
C | T | 1 | a0001c0001t0008g0208 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1678+276C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135128 | ||||||
| chr12:125135233
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1678+381G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135233 | ||||||
| chr12:125135337
|
C | T | 13 | a0001c0001t0005g0060a0001c0001t0005g0072a0001c0001t0005g0099others(10): Show | 13 | HG01515.hp2 HG01928.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1678+485C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135337 | ||||||
| chr12:125135518
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1678+666A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135518 | ||||||
| chr12:125135748
|
T | A | 6 | a0001c0001t0001g0039a0001c0009t0001g0348a0001c0009t0001g0349others(3): Show | 6 | HG01168.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+896T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135748 | ||||||
| chr12:125135756
|
T | A | 4 | a0001c0001t0001g0079a0001c0015t0001g0070a0002c0010t0001g0018others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+904T>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135756 | ||||||
| chr12:125135890
|
C | T | 4 | a0001c0003t0001g0214a0001c0003t0001g0217a0001c0003t0001g0236others(1): Show | 4 | HG00621.hp1 HG02080.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-772C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135890 | ||||||
| chr12:125135946
|
A | T | 1 | a0002c0005t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1679-716A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125135946 | ||||||
| chr12:125136021
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0162others(15): Show | 18 | HG00558.hp2 HG01243.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.1679-641C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125136021 | ||||||
| chr12:125136127
|
G | A | 2 | a0002c0011t0001g0014a0002c0021t0001g0026 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1679-535G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125136127 | ||||||
| chr12:125136174
|
C | T | 1 | a0002c0005t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1679-488C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125136174 | ||||||
| chr12:125136467
|
C | T | 32 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1679-195C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125136467 | ||||||
| chr12:125136520
|
T | C | 182 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0033others(179): Show | 184 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.1679-142T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 16/17 | chr12 | 125136520 | ||||||
| chr12:125136873
|
A | G | 139 | a0001c0001t0001g0010a0001c0001t0001g0039a0001c0001t0001g0091others(136): Show | 140 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1881+9A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125136873 | ||||||
| chr12:125136891
|
G | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02922.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1881+27G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125136891 | ||||||
| chr12:125137259
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1881+395C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137259 | ||||||
| chr12:125137382
|
A | G | 3 | a0001c0001t0002g0188a0001c0001t0002g0201a0001c0001t0002g0253 | 3 | HG00735.hp1 HG01981.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1881+518A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137382 | ||||||
| chr12:125137425
|
G | A | 28 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(25): Show | 28 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1881+561G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137425 | ||||||
| chr12:125137457
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1881+593C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137457 | ||||||
| chr12:125137514
|
G | A | 5 | a0001c0001t0002g0081a0001c0001t0002g0205a0001c0001t0002g0206others(2): Show | 5 | HG00140.hp2 HG01192.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1881+650G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137514 | ||||||
| chr12:125137520
|
G | A | 32 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1881+656G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137520 | ||||||
| chr12:125137716
|
G | A | 138 | a0001c0001t0001g0010a0001c0001t0001g0039a0001c0001t0001g0091others(135): Show | 139 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.1881+852G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137716 | ||||||
| chr12:125137731
|
C | A | 5 | a0001c0001t0005g0048a0002c0002t0001g0004a0002c0002t0001g0264others(2): Show | 6 | HG01243.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1881+867C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137731 | ||||||
| chr12:125137734
|
CTGTGTG | C | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1881+877_1881+882d others(8): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125137734 | |||||
| chr12:125137825
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1881+961G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137825 | ||||||
| chr12:125137944
|
T | G | 7 | a0001c0001t0001g0079a0001c0015t0001g0070a0002c0007t0001g0016others(4): Show | 7 | HG01175.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1881+1080T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137944 | ||||||
| chr12:125137962
|
T | C | 1 | a0002c0002t0001g0131 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1881+1098T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137962 | ||||||
| chr12:125137979
|
G | A | 1 | a0002c0002t0001g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1881+1115G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125137979 | ||||||
| chr12:125138007
|
CT | C | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1881+1146delT | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125138007 | |||||
| chr12:125138083
|
C | T | 32 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0109others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1881+1219C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138083 | ||||||
| chr12:125138143
|
TCCTCCTC others(50): Show |
T | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1881+1300_1881+135 others(61): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125138143 | |||||
| chr12:125138317
|
A | T | 1 | a0001c0001t0006g0084 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1881+1453A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138317 | ||||||
| chr12:125138515
|
C | A | 1 | a0001c0001t0002g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1881+1651C>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138515 | ||||||
| chr12:125138594
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1881+1730G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138594 | ||||||
| chr12:125138748
|
A | G | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1881+1884A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138748 | ||||||
| chr12:125138794
|
C | T | 3 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0009 | 3 | HG02145.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1881+1930C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138794 | ||||||
| chr12:125138852
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0162others(15): Show | 18 | HG01243.hp1 HG01361.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1881+1988G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138852 | ||||||
| chr12:125138866
|
C | T | 5 | a0001c0001t0005g0048a0002c0002t0001g0004a0002c0002t0001g0264others(2): Show | 6 | HG01243.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1881+2002C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138866 | ||||||
| chr12:125138882
|
C | T | 1 | a0002c0006t0001g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1881+2018C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125138882 | ||||||
| chr12:125138904
|
A | AGGAACTG others(16): Show |
79 | a0001c0001t0001g0039a0001c0001t0001g0161a0001c0001t0001g0169others(76): Show | 80 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1881+2041_1881+206 others(27): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125138904 | |||||
| chr12:125138905
|
G | GGAACTGG others(16): Show |
9 | a0001c0001t0002g0045a0001c0001t0002g0181a0001c0001t0002g0183others(6): Show | 9 | HG00544.hp1 NA18952.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.1881+2045_1881+206 others(27): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125138905 | |||||
| chr12:125139198
|
A | T | 1 | a0002c0002t0001g0135 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1881+2334A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139198 | ||||||
| chr12:125139226
|
A | G | 1 | a0002c0002t0001g0001 | 2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1881+2362A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139226 | ||||||
| chr12:125139309
|
C | T | 9 | a0001c0001t0001g0327a0002c0002t0001g0121a0002c0002t0001g0130others(6): Show | 9 | HG00621.hp2 NA18954.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.1881+2445C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139309 | ||||||
| chr12:125139341
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1881+2477C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139341 | ||||||
| chr12:125139456
|
A | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG01175.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1881+2592A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139456 | ||||||
| chr12:125139499
|
A | T | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1882-2593A>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139499 | ||||||
| chr12:125139500
|
C | G | 3 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0027 | 3 | HG02280.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1882-2592C>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139500 | ||||||
| chr12:125139603
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02922.hp2 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882-2489G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139603 | ||||||
| chr12:125139774
|
G | T | 106 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(103): Show | 108 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1882-2318G>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125139774 | ||||||
| chr12:125140017
|
G | A | 2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1882-2075G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125140017 | ||||||
| chr12:125140069
|
G | A | 2 | a0002c0002t0001g0273a0002c0002t0001g0274 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1882-2023G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125140069 | ||||||
| chr12:125140125
|
G | A | 8 | a0001c0001t0005g0063a0001c0001t0005g0105a0001c0001t0005g0106others(5): Show | 8 | HG00140.hp1 HG01515.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1882-1967G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125140125 | ||||||
| chr12:125140311
|
C | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0093others(29): Show | 32 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1882-1781C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125140311 | ||||||
| chr12:125140564
|
G | A | 4 | a0001c0001t0005g0060a0001c0001t0005g0072a0001c0001t0005g0099others(1): Show | 4 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882-1528G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125140564 | ||||||
| chr12:125140567
|
G | A | 20 | a0001c0003t0004g0083a0001c0004t0001g0212a0001c0004t0001g0213others(17): Show | 20 | HG00544.hp2 HG00597.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1882-1525G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125140567 | ||||||
| chr12:125140609
|
T | TA | 20 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0093others(17): Show | 20 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1882-1470dupA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125140609 | |||||
| chr12:125140609
|
TA | T | 6 | a0001c0001t0001g0291a0001c0001t0002g0231a0001c0001t0003g0276others(3): Show | 6 | NA18942.hp1 NA18949.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1882-1470delA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125140609 | |||||
| chr12:125140963
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1882-1129A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125140963 | ||||||
| chr12:125141024
|
A | G | 185 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0039others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1882-1068A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141024 | ||||||
| chr12:125141057
|
T | C | 185 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0039others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1882-1035T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141057 | ||||||
| chr12:125141223
|
C | T | 7 | a0001c0001t0001g0239a0001c0001t0001g0284a0001c0001t0001g0294others(4): Show | 7 | HG01943.hp1 HG03017.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1882-869C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141223 | ||||||
| chr12:125141481
|
T | C | 4 | a0001c0001t0001g0079a0001c0015t0001g0070a0002c0010t0001g0018others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1882-611T>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141481 | ||||||
| chr12:125141500
|
CAT | C | 42 | a0001c0001t0001g0028a0001c0003t0001g0168a0001c0003t0001g0210others(39): Show | 42 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1882-591_1882-590d others(4): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141500 | ||||||
| chr12:125141615
|
T | G | 1 | a0001c0003t0001g0217 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1882-477T>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141615 | ||||||
| chr12:125141628
|
G | C | 180 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0039others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1882-464G>C | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141628 | ||||||
| chr12:125141644
|
C | T | 15 | a0001c0001t0005g0048a0001c0001t0005g0060a0001c0001t0005g0063others(12): Show | 15 | HG00140.hp1 HG01515.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.1882-448C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141644 | ||||||
| chr12:125141701
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1882-373_1882-364d others(12): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125141701 | |||||
| chr12:125141706
|
AAAAAG | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0162others(13): Show | 16 | HG01243.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1882-381_1882-377d others(7): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125141706 | |||||
| chr12:125141708
|
AAAG | A | 76 | a0001c0001t0001g0169a0001c0001t0001g0196a0001c0001t0002g0002others(73): Show | 77 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1882-381_1882-379d others(5): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125141708 | |||||
| chr12:125141711
|
GAAAA | G | 17 | a0001c0001t0001g0039a0001c0001t0001g0091a0001c0001t0001g0093others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1882-375_1882-372d others(6): Show |
AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125141711 | |||||
| chr12:125141715
|
A | G | 94 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0162others(91): Show | 95 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1882-377A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141715 | ||||||
| chr12:125141719
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0002g0286 | 2 | HG01943.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1882-373A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141719 | ||||||
| chr12:125141721
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1882-371G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141721 | ||||||
| chr12:125141731
|
A | G | 18 | a0001c0001t0005g0048a0001c0001t0005g0060a0001c0001t0005g0063others(15): Show | 18 | HG00140.hp1 HG01515.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.1882-361A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141731 | ||||||
| chr12:125141806
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0002g0223 | 3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1882-286G>A | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141806 | ||||||
| chr12:125141855
|
GA | G | 173 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0039others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1882-234delA | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 125141855 | |||||
| chr12:125141916
|
C | T | 15 | a0001c0004t0004g0098a0001c0004t0004g0167a0001c0004t0004g0209others(12): Show | 15 | HG00544.hp2 HG00597.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1882-176C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141916 | ||||||
| chr12:125141968
|
C | T | 1 | a0001c0001t0005g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1882-124C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141968 | ||||||
| chr12:125141989
|
A | G | 179 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0039others(176): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.1882-103A>G | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125141989 | ||||||
| chr12:125142036
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1882-56C>T | AACS | ENSG00000081760.17 | transcript | ENST00000316519.11 | protein_coding | 17/17 | chr12 | 125142036 |