Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84324 |
|---|---|
| ensemblid | ENSG00000205323.9 |
| hgncid | 24432 |
| symbol | SARNP |
| name | SAP domain containing ribonucleoprotein |
| refseq_nuc | NM_033082.4 |
| refseq_prot | NP_149073.1 |
| ensembl_nuc | ENST00000336133.8 |
| ensembl_prot | ENSP00000337632.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 55757270 |
| end | 55817724 |
| strand | - |
| ver | v1.2 |
| region | chr12:55757270-55817724 |
| region5000 | chr12:55752270-55822724 |
| regionname0 | SARNP_chr12_55757270_55817724 |
| regionname5000 | SARNP_chr12_55752270_55822724 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 210 | 274 | 92 | 52 | 94 | 6 | 28 | 64 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| a0002 | 0/0 | 210 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 633 | 274 | 92 | 52 | 94 | 6 | 28 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| c0002 | 0/0 | 633 | 2 | 0 | 0 | 2 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| 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 | 1/1 | 266 | 231 | 87 | 36 | 77 | 4 | 25 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| t0002 | 0/0 | 266 | 40 | 2 | 15 | 18 | 2 | 3 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| t0003 | 0/0 | 266 | 4 | 3 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| t0004 | 0/0 | 266 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0004 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0073 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 633 | 274 | 92 | 52 | 94 | 6 | 28 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| a0002c0002 | 0/0 | 633 | 2 | 0 | 0 | 2 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 898 | 229 | 87 | 36 | 75 | 4 | 25 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| a0001c0001t0002 | 0/0 | 898 | 40 | 2 | 15 | 18 | 2 | 3 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| a0001c0001t0003 | 0/0 | 898 | 4 | 3 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| a0001c0001t0004 | 0/0 | 898 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| a0002c0002t0001 | 0/0 | 898 | 2 | 0 | 0 | 2 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | copy fasta | chr12 | 55752270 | 55822724 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0073 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0186 | EUR | FIN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ASW | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | TSI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | GIH | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | USA | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | USA | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0103 | REF | REF | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0073 | REF | REF | SARNP_chr12_55752270_55822724 | SARNP | chr12 | 55752270 | 55822724 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:55800583
|
G | A | 1 | a0002 | 2 | NA18965.hp2 NA19074.hp1 |
missense_variant | MODERATE | c.230C>T | p.Pro77Leu | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/11 | 253/898 | 230/633 | 77/210 | chr12 | 55800583 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:55757314
|
A | C | 1 | a0001c0001t0004 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 11/11 | 198 | chr12 | 55757314 | |||||
| chr12:55757365
|
C | T | 1 | a0001c0001t0003 | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*147G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 11/11 | 147 | chr12 | 55757365 | |||||
| chr12:55757507
|
T | C | 2 | a0001c0001t0002a0001c0001t0004 | 41 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*5A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 11/11 | 5 | chr12 | 55757507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:55758032
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.592-479T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758032 | ||||||
| chr12:55758055
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0123a0001c0001t0001g0161others(1): Show | 4 | NA18961.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-502T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758055 | ||||||
| chr12:55758150
|
G | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0062 | 3 | HG02451.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.592-597C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758150 | ||||||
| chr12:55758164
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.592-611C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758164 | ||||||
| chr12:55758176
|
C | G | 34 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(31): Show | 34 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.592-623G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758176 | ||||||
| chr12:55758290
|
G | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.592-737C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758290 | ||||||
| chr12:55758631
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.592-1078G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758631 | ||||||
| chr12:55758644
|
C | CA | 6 | a0001c0001t0001g0026a0001c0001t0001g0053a0001c0001t0003g0065others(3): Show | 6 | HG01243.hp2 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.592-1092dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758644 | ||||||
| chr12:55758651
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.592-1098T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758651 | ||||||
| chr12:55758905
|
C | CT | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00423.hp1 HG00741.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.592-1353dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758905 | ||||||
| chr12:55758905
|
CT | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0018others(17): Show | 20 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.592-1353delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758905 | ||||||
| chr12:55758924
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.592-1371A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758924 | ||||||
| chr12:55758962
|
G | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 275 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.592-1409C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55758962 | ||||||
| chr12:55759046
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.592-1493A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55759046 | ||||||
| chr12:55759284
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0062others(1): Show | 4 | HG02451.hp1 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+1267A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55759284 | ||||||
| chr12:55759335
|
T | C | 1 | a0001c0001t0004g0132 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.591+1216A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55759335 | ||||||
| chr12:55759419
|
CT | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG01891.hp1 HG01943.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+1131delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55759419 | ||||||
| chr12:55759504
|
G | A | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.591+1047C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55759504 | ||||||
| chr12:55759711
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.591+840C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55759711 | ||||||
| chr12:55759716
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.591+835A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 10/10 | chr12 | 55759716 | ||||||
| chr12:55760782
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.502-142T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55760782 | ||||||
| chr12:55760879
|
TAAAG | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-243_502-240del others(4): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55760879 | ||||||
| chr12:55761009
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502-369C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55761009 | ||||||
| chr12:55761067
|
C | G | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.502-427G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55761067 | ||||||
| chr12:55761074
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA19011.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.502-434C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55761074 | ||||||
| chr12:55761373
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.502-733T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55761373 | ||||||
| chr12:55761819
|
G | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244 | 3 | HG02723.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.502-1179C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55761819 | ||||||
| chr12:55761833
|
C | T | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-1193G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55761833 | ||||||
| chr12:55762114
|
C | T | 20 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(17): Show | 20 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.502-1474G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55762114 | ||||||
| chr12:55762305
|
C | CT | 34 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0049others(31): Show | 34 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.502-1666dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55762305 | ||||||
| chr12:55762461
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.502-1821C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55762461 | ||||||
| chr12:55762515
|
G | A | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.502-1875C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55762515 | ||||||
| chr12:55763060
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.502-2420A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55763060 | ||||||
| chr12:55763308
|
C | CT | 73 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(70): Show | 73 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.502-2669dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55763308 | ||||||
| chr12:55763308
|
CT | C | 10 | a0001c0001t0001g0113a0001c0001t0001g0121a0001c0001t0001g0146others(7): Show | 10 | HG01071.hp2 HG01243.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.502-2669delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55763308 | ||||||
| chr12:55763324
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 140 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.502-2684A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55763324 | ||||||
| chr12:55763350
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.502-2710G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55763350 | ||||||
| chr12:55763351
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.502-2711C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55763351 | ||||||
| chr12:55763551
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.502-2911C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55763551 | ||||||
| chr12:55764081
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.502-3441G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764081 | ||||||
| chr12:55764304
|
T | G | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502-3664A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764304 | ||||||
| chr12:55764531
|
C | CA | 9 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0072others(6): Show | 10 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.502-3892dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764531 | ||||||
| chr12:55764607
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502-3967G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764607 | ||||||
| chr12:55764608
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(131): Show | 135 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.502-3968T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764608 | ||||||
| chr12:55764764
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0200 | 2 | HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.502-4124C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764764 | ||||||
| chr12:55764832
|
C | CA | 24 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0098others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.502-4193dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764832 | ||||||
| chr12:55764832
|
CA | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(39): Show | 43 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.502-4193delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764832 | ||||||
| chr12:55764832
|
CAA | C | 15 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0057others(12): Show | 15 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.502-4194_502-4193d others(4): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764832 | ||||||
| chr12:55764855
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0213a0001c0001t0001g0268 | 3 | HG01099.hp1 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.502-4215C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764855 | ||||||
| chr12:55764899
|
CAAAGTCA others(7): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.502-4273_502-4260d others(16): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55764899 | ||||||
| chr12:55765203
|
A | G | 5 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0164others(2): Show | 5 | HG00544.hp2 HG02135.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-4563T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55765203 | ||||||
| chr12:55765264
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG01255.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.502-4624G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55765264 | ||||||
| chr12:55765509
|
AT | A | 22 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0040others(19): Show | 22 | HG01257.hp1 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.502-4870delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55765509 | ||||||
| chr12:55765857
|
C | CAACTGGG others(4): Show |
1 | a0001c0001t0001g0048 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.502-5228_502-5218d others(13): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55765857 | ||||||
| chr12:55766616
|
C | CG | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(37): Show | 44 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.502-5977dupC | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766616
|
C | CGG | 17 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0104others(14): Show | 17 | HG00408.hp2 HG01071.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.502-5978_502-5977d others(4): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766616
|
C | CGGGGGGG others(3): Show |
1 | a0001c0001t0001g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.502-5986_502-5977d others(12): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766616
|
C | CGGGGGGG others(4): Show |
1 | a0001c0001t0001g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.502-5987_502-5977d others(13): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766616
|
C | CGGGGGGG others(5): Show |
1 | a0001c0001t0001g0038 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.502-5988_502-5977d others(14): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766616
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.502-5976G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766616
|
CG | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(48): Show | 52 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.502-5977delC | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766616
|
CGG | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0014others(38): Show | 41 | HG01258.hp2 HG01433.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.502-5978_502-5977d others(4): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766616
|
CGGG | C | 22 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0030others(19): Show | 22 | HG01255.hp1 HG01975.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.502-5979_502-5977d others(5): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766616 | ||||||
| chr12:55766624
|
G | T | 1 | a0001c0001t0001g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.502-5984C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766624 | ||||||
| chr12:55766878
|
GCCTAGTC others(7): Show |
G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 264 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.502-6252_502-6239d others(16): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55766878 | ||||||
| chr12:55767064
|
A | G | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG01255.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.502-6424T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767064 | ||||||
| chr12:55767075
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.502-6435G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767075 | ||||||
| chr12:55767314
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.502-6674C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767314 | ||||||
| chr12:55767383
|
C | CA | 14 | a0001c0001t0001g0038a0001c0001t0001g0101a0001c0001t0001g0140others(11): Show | 14 | HG01175.hp1 HG01175.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.502-6744dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767383 | ||||||
| chr12:55767441
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.502-6801G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767441 | ||||||
| chr12:55767644
|
G | A | 41 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0012others(38): Show | 41 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.502-7004C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767644 | ||||||
| chr12:55767663
|
C | T | 1 | a0001c0001t0001g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.502-7023G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767663 | ||||||
| chr12:55767664
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.502-7024C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767664 | ||||||
| chr12:55767686
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.502-7046T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767686 | ||||||
| chr12:55767708
|
A | G | 49 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(46): Show | 49 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.502-7068T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767708 | ||||||
| chr12:55767848
|
G | GA | 13 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0112others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.502-7209dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767848 | ||||||
| chr12:55767848
|
GA | G | 113 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(110): Show | 113 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.502-7209delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55767848 | ||||||
| chr12:55768195
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.502-7555C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55768195 | ||||||
| chr12:55768331
|
T | C | 2 | a0001c0001t0002g0130a0001c0001t0002g0200 | 2 | HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.502-7691A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55768331 | ||||||
| chr12:55768500
|
C | A | 1 | a0001c0001t0003g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.502-7860G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55768500 | ||||||
| chr12:55768632
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.502-7992G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55768632 | ||||||
| chr12:55768664
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.502-8024C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55768664 | ||||||
| chr12:55768793
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.502-8153C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55768793 | ||||||
| chr12:55769002
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG00735.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.502-8362G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55769002 | ||||||
| chr12:55769116
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.502-8476A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55769116 | ||||||
| chr12:55769258
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502-8618C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55769258 | ||||||
| chr12:55769452
|
C | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(202): Show | 206 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.502-8812G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55769452 | ||||||
| chr12:55769905
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.502-9265A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55769905 | ||||||
| chr12:55769950
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(131): Show | 135 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.502-9310C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55769950 | ||||||
| chr12:55770227
|
AT | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0069others(5): Show | 8 | HG01361.hp2 HG02280.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-9588delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770227 | ||||||
| chr12:55770264
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.502-9624G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770264 | ||||||
| chr12:55770394
|
G | GT | 31 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0032others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.502-9755dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770394 | ||||||
| chr12:55770491
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0165 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.502-9851T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770491 | ||||||
| chr12:55770508
|
T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(131): Show | 135 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.502-9868A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770508 | ||||||
| chr12:55770589
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502-9949A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770589 | ||||||
| chr12:55770640
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502-10000A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770640 | ||||||
| chr12:55770936
|
C | CT | 6 | a0001c0001t0001g0048a0001c0001t0001g0112a0001c0001t0001g0210others(3): Show | 6 | HG00741.hp2 HG02080.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-10297dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770936 | ||||||
| chr12:55770936
|
CT | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0026others(26): Show | 29 | HG00323.hp2 HG01433.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.502-10297delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55770936 | ||||||
| chr12:55771078
|
C | G | 1 | a0001c0001t0002g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.502-10438G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55771078 | ||||||
| chr12:55771082
|
C | A | 1 | a0001c0001t0002g0005 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.502-10442G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55771082 | ||||||
| chr12:55771714
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.502-11074A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55771714 | ||||||
| chr12:55771776
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.502-11136C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55771776 | ||||||
| chr12:55772037
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG02622.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-11397G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772037 | ||||||
| chr12:55772165
|
A | G | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.502-11525T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772165 | ||||||
| chr12:55772352
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.502-11712G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772352 | ||||||
| chr12:55772483
|
A | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 275 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.502-11843T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772483 | ||||||
| chr12:55772659
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.502-12019T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772659 | ||||||
| chr12:55772712
|
C | CT | 198 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(195): Show | 199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.502-12073dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772712 | ||||||
| chr12:55772771
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.502-12131T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772771 | ||||||
| chr12:55772802
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.502-12162G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772802 | ||||||
| chr12:55772961
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.502-12321G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772961 | ||||||
| chr12:55772967
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.502-12327C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55772967 | ||||||
| chr12:55773681
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.502-13041T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55773681 | ||||||
| chr12:55773774
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.502-13134C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55773774 | ||||||
| chr12:55774454
|
TCATGCCT others(3): Show |
T | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502-13824_502-1381 others(14): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774454 | ||||||
| chr12:55774466
|
T | G | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502-13826A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774466 | ||||||
| chr12:55774467
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502-13827G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774467 | ||||||
| chr12:55774534
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502-13894C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774534 | ||||||
| chr12:55774558
|
T | TAAAAAAA | 4 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0082others(1): Show | 4 | HG01175.hp1 HG01361.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-13919_502-1391 others(11): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(5): Show |
3 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0038 | 3 | HG02451.hp2 HG02615.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.502-13919_502-1391 others(16): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(7): Show |
5 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0037others(2): Show | 5 | HG02486.hp1 HG02735.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-13919_502-1391 others(18): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.502-13919_502-1391 others(19): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.502-13919_502-1391 others(20): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0001g0041 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.502-13919_502-1391 others(22): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG00733.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.502-13919_502-1391 others(23): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(13): Show |
1 | a0001c0001t0001g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.502-13919_502-1391 others(24): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(14): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0052 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.502-13919_502-1391 others(25): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.502-13919_502-1391 others(27): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
T | TAAAAAAA others(28): Show |
1 | a0001c0001t0001g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.502-13919_502-1391 others(39): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774558
|
TG | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(78): Show | 82 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.502-13919delC | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774558 | ||||||
| chr12:55774559
|
G | A | 52 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(49): Show | 52 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.502-13919C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774559 | ||||||
| chr12:55774559
|
GA | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.502-13920delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774559 | ||||||
| chr12:55774566
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.502-13939_502-1392 others(17): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774566 | ||||||
| chr12:55774570
|
A | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0072others(4): Show | 8 | HG02572.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.502-13930T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774570 | ||||||
| chr12:55774571
|
A | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0115others(6): Show | 11 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.502-13931T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774571 | ||||||
| chr12:55774575
|
C | A | 33 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(30): Show | 33 | HG00733.hp2 HG01175.hp1 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.502-13935G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774575 | ||||||
| chr12:55774577
|
A | C | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0220 | 3 | HG01978.hp1 NA19000.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.502-13937T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774577 | ||||||
| chr12:55774577
|
AAC | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(60): Show | 63 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.502-13939_502-1393 others(6): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774577 | ||||||
| chr12:55774578
|
AC | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0025others(19): Show | 23 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.502-13939delG | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774578 | ||||||
| chr12:55774579
|
C | A | 33 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(30): Show | 33 | HG00733.hp2 HG01175.hp1 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.502-13939G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774579 | ||||||
| chr12:55774579
|
CA | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.502-13940delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774579 | ||||||
| chr12:55774593
|
C | A | 17 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0042others(14): Show | 17 | HG01361.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.502-13953G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774593 | ||||||
| chr12:55774883
|
G | GT | 121 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(118): Show | 121 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.501+14191dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774883 | ||||||
| chr12:55774883
|
G | GTT | 10 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0046others(7): Show | 10 | HG01978.hp1 HG02055.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.501+14190_501+1419 others(6): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774883 | ||||||
| chr12:55774892
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.501+14183A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774892 | ||||||
| chr12:55774902
|
T | TG | 3 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074 | 4 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+14172dupC | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774902 | ||||||
| chr12:55774948
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.501+14127C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774948 | ||||||
| chr12:55774982
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.501+14093C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55774982 | ||||||
| chr12:55775241
|
T | TA | 52 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0031others(49): Show | 52 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.501+13833dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775241 | ||||||
| chr12:55775241
|
T | TAA | 60 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0025others(57): Show | 61 | HG00423.hp1 HG00438.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.501+13832_501+1383 others(6): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775241 | ||||||
| chr12:55775241
|
T | TAAA | 49 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0215others(46): Show | 49 | HG00323.hp1 HG00621.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.501+13831_501+1383 others(7): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775241 | ||||||
| chr12:55775377
|
TG | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 275 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.501+13697delC | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775377 | ||||||
| chr12:55775497
|
AT | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 275 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.501+13577delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775497 | ||||||
| chr12:55775535
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.501+13540T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775535 | ||||||
| chr12:55775555
|
C | CA | 42 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(39): Show | 42 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.501+13519dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775555 | ||||||
| chr12:55775561
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.501+13514T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775561 | ||||||
| chr12:55775595
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.501+13480C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775595 | ||||||
| chr12:55775627
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.501+13448T>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775627 | ||||||
| chr12:55775704
|
T | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02965.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.501+13371A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55775704 | ||||||
| chr12:55776004
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG00733.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.501+13071A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55776004 | ||||||
| chr12:55776394
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.501+12681G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55776394 | ||||||
| chr12:55776438
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.501+12637G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55776438 | ||||||
| chr12:55776485
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074 | 4 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+12590G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55776485 | ||||||
| chr12:55776514
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.501+12561A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55776514 | ||||||
| chr12:55776558
|
T | G | 3 | a0001c0001t0001g0163a0001c0001t0001g0213a0001c0001t0001g0268 | 3 | HG01099.hp1 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.501+12517A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55776558 | ||||||
| chr12:55776991
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 7 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.501+12084C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55776991 | ||||||
| chr12:55777109
|
A | G | 32 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(29): Show | 32 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.501+11966T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55777109 | ||||||
| chr12:55777494
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.501+11581G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55777494 | ||||||
| chr12:55777548
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074 | 4 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+11527C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55777548 | ||||||
| chr12:55777717
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.501+11358G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55777717 | ||||||
| chr12:55777802
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0182others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+11273A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55777802 | ||||||
| chr12:55778013
|
C | G | 6 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0164others(3): Show | 6 | HG00544.hp2 HG02135.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+11062G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778013 | ||||||
| chr12:55778123
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.501+10952A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778123 | ||||||
| chr12:55778233
|
A | G | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.501+10842T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778233 | ||||||
| chr12:55778515
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.501+10560A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778515 | ||||||
| chr12:55778529
|
T | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+10546A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778529 | ||||||
| chr12:55778729
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.501+10346A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778729 | ||||||
| chr12:55778759
|
C | T | 6 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0164others(3): Show | 6 | HG00544.hp2 HG02135.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+10316G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778759 | ||||||
| chr12:55778813
|
T | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+10262A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778813 | ||||||
| chr12:55778979
|
G | GCAAAA | 3 | a0001c0001t0001g0094a0001c0001t0001g0140a0001c0001t0001g0165 | 3 | HG02818.hp2 HG03471.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.501+10091_501+1009 others(9): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778979 | ||||||
| chr12:55778979
|
GCAAAA | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0231 | 3 | HG02717.hp1 HG03540.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.501+10091_501+1009 others(9): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55778979 | ||||||
| chr12:55779255
|
G | T | 1 | a0001c0001t0002g0131 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.501+9820C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55779255 | ||||||
| chr12:55779317
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.501+9758G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55779317 | ||||||
| chr12:55779519
|
C | G | 1 | a0001c0001t0002g0111 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.501+9556G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55779519 | ||||||
| chr12:55779792
|
T | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.501+9283A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55779792 | ||||||
| chr12:55779972
|
C | A | 1 | a0001c0001t0001g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.501+9103G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55779972 | ||||||
| chr12:55779974
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.501+9101G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55779974 | ||||||
| chr12:55780184
|
G | A | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0182others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+8891C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55780184 | ||||||
| chr12:55780362
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074 | 4 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+8713C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55780362 | ||||||
| chr12:55780494
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.501+8581T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55780494 | ||||||
| chr12:55780511
|
G | GA | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.501+8563dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55780511 | ||||||
| chr12:55780705
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074 | 4 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+8370G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55780705 | ||||||
| chr12:55780937
|
G | T | 8 | a0001c0001t0001g0092a0001c0001t0001g0112a0001c0001t0001g0142others(5): Show | 8 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.501+8138C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55780937 | ||||||
| chr12:55781044
|
C | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+8031G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55781044 | ||||||
| chr12:55781209
|
T | G | 17 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 17 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.501+7866A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55781209 | ||||||
| chr12:55781287
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.501+7788A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55781287 | ||||||
| chr12:55781341
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.501+7734G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55781341 | ||||||
| chr12:55781533
|
C | CA | 14 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 14 | HG01175.hp1 HG01255.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.501+7541dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55781533 | ||||||
| chr12:55781533
|
CA | C | 66 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(63): Show | 66 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.501+7541delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55781533 | ||||||
| chr12:55781543
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.501+7532T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55781543 | ||||||
| chr12:55782081
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.501+6994A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55782081 | ||||||
| chr12:55782392
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.501+6683T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55782392 | ||||||
| chr12:55782412
|
T | C | 5 | a0001c0001t0001g0053a0001c0001t0003g0065a0001c0001t0003g0066others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+6663A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55782412 | ||||||
| chr12:55782439
|
C | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0240 | 2 | HG02040.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.501+6636G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55782439 | ||||||
| chr12:55782440
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0240 | 2 | HG02040.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.501+6635G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55782440 | ||||||
| chr12:55782624
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0165 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.501+6451A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55782624 | ||||||
| chr12:55782665
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.501+6410G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55782665 | ||||||
| chr12:55782979
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.501+6096G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55782979 | ||||||
| chr12:55783010
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.501+6065G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55783010 | ||||||
| chr12:55783183
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.501+5892G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55783183 | ||||||
| chr12:55783228
|
A | G | 1 | a0001c0001t0002g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.501+5847T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55783228 | ||||||
| chr12:55783445
|
C | T | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.501+5630G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55783445 | ||||||
| chr12:55784091
|
CAG | C | 12 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0101others(9): Show | 12 | HG00544.hp2 HG02135.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+4982_501+4983d others(4): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784091 | ||||||
| chr12:55784170
|
T | G | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.501+4905A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784170 | ||||||
| chr12:55784249
|
T | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0240 | 2 | HG02040.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.501+4826A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784249 | ||||||
| chr12:55784367
|
G | A | 32 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(29): Show | 32 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.501+4708C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784367 | ||||||
| chr12:55784371
|
C | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074 | 4 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+4704G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784371 | ||||||
| chr12:55784470
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+4605G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784470 | ||||||
| chr12:55784632
|
G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074 | 4 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+4443C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784632 | ||||||
| chr12:55784648
|
G | A | 8 | a0001c0001t0001g0092a0001c0001t0001g0112a0001c0001t0001g0142others(5): Show | 8 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.501+4427C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784648 | ||||||
| chr12:55784739
|
A | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.501+4336T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784739 | ||||||
| chr12:55784751
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG02132.hp2 NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.501+4324C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784751 | ||||||
| chr12:55784846
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG00733.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.501+4229A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55784846 | ||||||
| chr12:55785120
|
TAATC | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074 | 4 | HG02630.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+3951_501+3954d others(6): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55785120 | ||||||
| chr12:55785411
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.501+3664T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55785411 | ||||||
| chr12:55785491
|
T | G | 1 | a0001c0001t0001g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.501+3584A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55785491 | ||||||
| chr12:55785518
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.501+3557C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55785518 | ||||||
| chr12:55785564
|
T | TG | 73 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(70): Show | 73 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.501+3510dupC | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55785564 | ||||||
| chr12:55785849
|
C | A | 5 | a0001c0001t0001g0053a0001c0001t0003g0065a0001c0001t0003g0066others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+3226G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55785849 | ||||||
| chr12:55785992
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.501+3083G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55785992 | ||||||
| chr12:55786012
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.501+3063T>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786012 | ||||||
| chr12:55786180
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.501+2895T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786180 | ||||||
| chr12:55786262
|
A | G | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(28): Show | 31 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.501+2813T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786262 | ||||||
| chr12:55786435
|
G | GGTTT | 39 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.501+2636_501+2639d others(6): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786435 | ||||||
| chr12:55786435
|
GGTTT | G | 58 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0116others(55): Show | 58 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.501+2636_501+2639d others(6): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786435 | ||||||
| chr12:55786435
|
GGTTTGTT others(1): Show |
G | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 5 | HG01361.hp1 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+2632_501+2639d others(10): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786435 | ||||||
| chr12:55786439
|
T | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0182others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+2636A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786439 | ||||||
| chr12:55786510
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0003g0065a0001c0001t0003g0066others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+2565G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786510 | ||||||
| chr12:55786606
|
C | G | 5 | a0001c0001t0001g0053a0001c0001t0003g0065a0001c0001t0003g0066others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+2469G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786606 | ||||||
| chr12:55786738
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+2337G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786738 | ||||||
| chr12:55786980
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(132): Show | 136 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.501+2095C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55786980 | ||||||
| chr12:55787241
|
T | TAAAAAA | 6 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0228others(3): Show | 6 | HG00323.hp1 HG01891.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+1828_501+1833d others(8): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55787241 | ||||||
| chr12:55787241
|
T | TAAAAAAA | 119 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 120 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.501+1827_501+1833d others(9): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55787241 | ||||||
| chr12:55787502
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0242others(2): Show | 5 | HG02723.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+1573A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55787502 | ||||||
| chr12:55787624
|
A | T | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.501+1451T>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55787624 | ||||||
| chr12:55787749
|
CT | C | 67 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(64): Show | 67 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.501+1325delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55787749 | ||||||
| chr12:55788251
|
T | C | 1 | a0001c0001t0001g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.501+824A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788251 | ||||||
| chr12:55788309
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.501+766C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788309 | ||||||
| chr12:55788342
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.501+733C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788342 | ||||||
| chr12:55788456
|
A | G | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG00741.hp1 HG02109.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.501+619T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788456 | ||||||
| chr12:55788575
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.501+500A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788575 | ||||||
| chr12:55788614
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.501+461A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788614 | ||||||
| chr12:55788689
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.501+386G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788689 | ||||||
| chr12:55788755
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.501+320C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788755 | ||||||
| chr12:55788837
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.501+238G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788837 | ||||||
| chr12:55788839
|
C | T | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | NA18956.hp2 NA18966.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+236G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55788839 | ||||||
| chr12:55789014
|
T | C | 3 | a0001c0001t0001g0208a0001c0001t0002g0137a0001c0001t0002g0138 | 3 | HG01175.hp1 HG01255.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.501+61A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55789014 | ||||||
| chr12:55789062
|
G | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 14 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+13C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 9/10 | chr12 | 55789062 | ||||||
| chr12:55789244
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.433-101A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55789244 | ||||||
| chr12:55789320
|
TG | T | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-178delC | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55789320 | ||||||
| chr12:55789943
|
C | CA | 14 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0085others(11): Show | 14 | HG00438.hp2 HG02818.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.432+623dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55789943 | ||||||
| chr12:55790008
|
C | G | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.432+559G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55790008 | ||||||
| chr12:55790172
|
T | A | 4 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG01255.hp1 HG01433.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+395A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55790172 | ||||||
| chr12:55790230
|
T | A | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.432+337A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55790230 | ||||||
| chr12:55790275
|
C | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 145 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.432+292G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55790275 | ||||||
| chr12:55790353
|
G | A | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+214C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55790353 | ||||||
| chr12:55790359
|
C | T | 54 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(51): Show | 54 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.432+208G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 8/10 | chr12 | 55790359 | ||||||
| chr12:55790689
|
C | G | 9 | a0001c0001t0001g0123a0001c0001t0002g0126a0001c0001t0002g0127others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-97G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55790689 | ||||||
| chr12:55790728
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.407-136A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55790728 | ||||||
| chr12:55790855
|
T | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.407-263A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55790855 | ||||||
| chr12:55791115
|
C | A | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-523G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791115 | ||||||
| chr12:55791423
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 217 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.407-831T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791423 | ||||||
| chr12:55791523
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.407-931G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791523 | ||||||
| chr12:55791651
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.407-1059G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791651 | ||||||
| chr12:55791686
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.407-1094G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791686 | ||||||
| chr12:55791694
|
CAAAAAAG others(1): Show |
C | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-1110_407-1103d others(10): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791694 | ||||||
| chr12:55791777
|
A | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 145 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.407-1185T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791777 | ||||||
| chr12:55791858
|
T | A | 1 | a0001c0001t0001g0004 | 2 | HG02735.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.407-1266A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791858 | ||||||
| chr12:55791860
|
C | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 14 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.407-1268G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55791860 | ||||||
| chr12:55792183
|
A | T | 1 | a0001c0001t0002g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.407-1591T>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55792183 | ||||||
| chr12:55792298
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.407-1706C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55792298 | ||||||
| chr12:55792344
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 271 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.407-1752C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55792344 | ||||||
| chr12:55792535
|
C | CT | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 150 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.406+1823dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55792535 | ||||||
| chr12:55792535
|
C | CTT | 13 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0001g0095others(10): Show | 13 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.406+1822_406+1823d others(4): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55792535 | ||||||
| chr12:55793310
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.406+1049A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55793310 | ||||||
| chr12:55793469
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.406+890G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55793469 | ||||||
| chr12:55793624
|
GA | G | 125 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(122): Show | 125 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.406+734delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55793624 | ||||||
| chr12:55793688
|
A | G | 42 | a0001c0001t0001g0123a0001c0001t0001g0208a0001c0001t0002g0005others(39): Show | 42 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.406+671T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55793688 | ||||||
| chr12:55794051
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0020 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.406+308A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55794051 | ||||||
| chr12:55794061
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.406+298A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55794061 | ||||||
| chr12:55794090
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.406+269C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55794090 | ||||||
| chr12:55794164
|
T | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+195A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 7/10 | chr12 | 55794164 | ||||||
| chr12:55794658
|
C | T | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.377+149G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 6/10 | chr12 | 55794658 | ||||||
| chr12:55794675
|
CA | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0182others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+131delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 6/10 | chr12 | 55794675 | ||||||
| chr12:55794957
|
T | TA | 45 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 45 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.304-78dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 5/10 | chr12 | 55794957 | ||||||
| chr12:55794957
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.304-89_304-78delTT others(10): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 5/10 | chr12 | 55794957 | ||||||
| chr12:55795301
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-421C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 5/10 | chr12 | 55795301 | ||||||
| chr12:55795439
|
A | C | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.304-559T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 5/10 | chr12 | 55795439 | ||||||
| chr12:55795581
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.303+444T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 5/10 | chr12 | 55795581 | ||||||
| chr12:55795955
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.303+70C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 5/10 | chr12 | 55795955 | ||||||
| chr12:55796228
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.252-152A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55796228 | ||||||
| chr12:55796563
|
G | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 271 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.252-487C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55796563 | ||||||
| chr12:55796651
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.252-575G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55796651 | ||||||
| chr12:55797169
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.252-1093A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55797169 | ||||||
| chr12:55797307
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.252-1231A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55797307 | ||||||
| chr12:55797464
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-1388G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55797464 | ||||||
| chr12:55797469
|
CCCATTTC others(4): Show |
C | 1 | a0001c0001t0002g0111 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.252-1404_252-1394d others(13): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55797469 | ||||||
| chr12:55797718
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.252-1642G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55797718 | ||||||
| chr12:55797808
|
T | C | 6 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(3): Show | 6 | HG01255.hp1 HG01433.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-1732A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55797808 | ||||||
| chr12:55797886
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.252-1810C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55797886 | ||||||
| chr12:55798159
|
T | A | 55 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(52): Show | 55 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.252-2083A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55798159 | ||||||
| chr12:55798262
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.252-2186G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55798262 | ||||||
| chr12:55798363
|
G | C | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0188others(1): Show | 4 | HG00544.hp1 HG02027.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2199C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55798363 | ||||||
| chr12:55798794
|
G | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.251+1768C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55798794 | ||||||
| chr12:55799086
|
A | G | 1 | a0001c0001t0002g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.251+1476T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799086 | ||||||
| chr12:55799195
|
T | A | 32 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(29): Show | 32 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.251+1367A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799195 | ||||||
| chr12:55799205
|
T | C | 5 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(2): Show | 5 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+1357A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799205 | ||||||
| chr12:55799431
|
C | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG00741.hp1 HG02109.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+1131G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799431 | ||||||
| chr12:55799449
|
A | C | 72 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(69): Show | 72 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.251+1113T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799449 | ||||||
| chr12:55799489
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.251+1073G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799489 | ||||||
| chr12:55799559
|
C | CTTTTT | 7 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0217others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.251+998_251+1002du others(6): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799559 | ||||||
| chr12:55799559
|
C | CTTTTTT | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 246 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.251+997_251+1002du others(7): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799559 | ||||||
| chr12:55799559
|
C | CTTTTTTT | 16 | a0001c0001t0001g0013a0001c0001t0001g0045a0001c0001t0001g0057others(13): Show | 16 | HG00408.hp2 HG00423.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.251+996_251+1002du others(8): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799559 | ||||||
| chr12:55799622
|
C | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251+940G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799622 | ||||||
| chr12:55799802
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.251+760A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799802 | ||||||
| chr12:55799954
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.251+608G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55799954 | ||||||
| chr12:55800010
|
T | C | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.251+552A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55800010 | ||||||
| chr12:55800107
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.251+455G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55800107 | ||||||
| chr12:55800190
|
C | CA | 14 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0058others(11): Show | 14 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.251+371dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 4/10 | chr12 | 55800190 | ||||||
| chr12:55800735
|
T | C | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.184-106A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 3/10 | chr12 | 55800735 | ||||||
| chr12:55800810
|
C | G | 5 | a0001c0001t0001g0053a0001c0001t0003g0065a0001c0001t0003g0066others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+44G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 3/10 | chr12 | 55800810 | ||||||
| chr12:55800905
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | splice_region_variant&intron_variant | LOW | c.137-5T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55800905 | ||||||
| chr12:55800975
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-75T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55800975 | ||||||
| chr12:55801076
|
C | A | 1 | a0001c0001t0001g0188 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.137-176G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55801076 | ||||||
| chr12:55801171
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG00733.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.137-271C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55801171 | ||||||
| chr12:55801218
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.137-318G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55801218 | ||||||
| chr12:55801219
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.137-319C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55801219 | ||||||
| chr12:55801258
|
C | T | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-358G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55801258 | ||||||
| chr12:55801705
|
C | A | 1 | a0001c0001t0001g0180 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.137-805G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55801705 | ||||||
| chr12:55801801
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 144 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.137-901T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55801801 | ||||||
| chr12:55801826
|
C | G | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.137-926G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55801826 | ||||||
| chr12:55802066
|
T | G | 19 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(16): Show | 19 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.137-1166A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55802066 | ||||||
| chr12:55802113
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.137-1213A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55802113 | ||||||
| chr12:55802474
|
C | T | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.136+1155G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55802474 | ||||||
| chr12:55802577
|
CAAAT | C | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+1048_136+1051d others(6): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55802577 | ||||||
| chr12:55802683
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.136+946C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55802683 | ||||||
| chr12:55802713
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0182others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+916T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55802713 | ||||||
| chr12:55802728
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136+901A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55802728 | ||||||
| chr12:55802925
|
T | TA | 7 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0181others(4): Show | 9 | HG00741.hp2 HG01081.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+703dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55802925 | ||||||
| chr12:55803408
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.136+221G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55803408 | ||||||
| chr12:55803494
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0072 | 3 | HG02647.hp2 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.136+135T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55803494 | ||||||
| chr12:55803610
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136+19C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 2/10 | chr12 | 55803610 | ||||||
| chr12:55803744
|
T | A | 1 | a0001c0001t0001g0266 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.37-16A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55803744 | ||||||
| chr12:55803838
|
A | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-110T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55803838 | ||||||
| chr12:55803917
|
G | A | 19 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(16): Show | 19 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.37-189C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55803917 | ||||||
| chr12:55803969
|
TCATCTAT others(8): Show |
T | 1 | a0001c0001t0001g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.37-256_37-242delGT others(13): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55803969 | ||||||
| chr12:55804069
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.37-341T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804069 | ||||||
| chr12:55804229
|
A | G | 4 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-501T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804229 | ||||||
| chr12:55804417
|
G | GA | 72 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(69): Show | 72 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.37-690dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804417 | ||||||
| chr12:55804417
|
GA | G | 12 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-690delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804417 | ||||||
| chr12:55804550
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02965.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.37-822C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804550 | ||||||
| chr12:55804652
|
T | C | 10 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.37-924A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804652 | ||||||
| chr12:55804708
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.37-980C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804708 | ||||||
| chr12:55804857
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.37-1129A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804857 | ||||||
| chr12:55804985
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.37-1257G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804985 | ||||||
| chr12:55804989
|
C | T | 2 | a0002c0002t0001g0033a0002c0002t0001g0034 | 2 | NA18965.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.37-1261G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804989 | ||||||
| chr12:55804996
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.37-1268C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55804996 | ||||||
| chr12:55805155
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.37-1427C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805155 | ||||||
| chr12:55805159
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.37-1431C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805159 | ||||||
| chr12:55805237
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.37-1509C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805237 | ||||||
| chr12:55805239
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.37-1511G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805239 | ||||||
| chr12:55805240
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.37-1512C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805240 | ||||||
| chr12:55805296
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.37-1568T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805296 | ||||||
| chr12:55805367
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.37-1639G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805367 | ||||||
| chr12:55805386
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.37-1658T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805386 | ||||||
| chr12:55805665
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.37-1937C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805665 | ||||||
| chr12:55805870
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.37-2142T>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55805870 | ||||||
| chr12:55806089
|
T | A | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(28): Show | 31 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.37-2361A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806089 | ||||||
| chr12:55806275
|
A | AT | 7 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0104others(4): Show | 7 | HG00741.hp2 HG02080.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.37-2548dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806275 | ||||||
| chr12:55806275
|
A | T | 1 | a0001c0001t0002g0111 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.37-2547T>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806275 | ||||||
| chr12:55806275
|
AT | A | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.37-2548delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806275 | ||||||
| chr12:55806276
|
T | A | 56 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(53): Show | 56 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.37-2548A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806276 | ||||||
| chr12:55806277
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.37-2549A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806277 | ||||||
| chr12:55806363
|
G | A | 3 | a0001c0001t0001g0214a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.37-2635C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806363 | ||||||
| chr12:55806447
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.37-2719C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806447 | ||||||
| chr12:55806511
|
G | A | 3 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0202 | 3 | HG00323.hp2 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.37-2783C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806511 | ||||||
| chr12:55806594
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.37-2866G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806594 | ||||||
| chr12:55806806
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.37-3078C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806806 | ||||||
| chr12:55806833
|
C | G | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.37-3105G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806833 | ||||||
| chr12:55806898
|
A | G | 1 | a0001c0001t0002g0110 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.37-3170T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806898 | ||||||
| chr12:55806917
|
A | G | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.37-3189T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806917 | ||||||
| chr12:55806982
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.37-3254C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55806982 | ||||||
| chr12:55807044
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.37-3316C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807044 | ||||||
| chr12:55807262
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.37-3534G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807262 | ||||||
| chr12:55807270
|
G | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(15): Show | 18 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.37-3542C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807270 | ||||||
| chr12:55807373
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.37-3645A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807373 | ||||||
| chr12:55807407
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 145 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.37-3679A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807407 | ||||||
| chr12:55807487
|
C | A | 1 | a0001c0001t0001g0254 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.37-3759G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807487 | ||||||
| chr12:55807529
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.37-3801C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807529 | ||||||
| chr12:55807531
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.37-3803C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807531 | ||||||
| chr12:55807646
|
C | CA | 51 | a0001c0001t0001g0075a0001c0001t0001g0104a0001c0001t0001g0190others(48): Show | 51 | HG00323.hp1 HG00621.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.37-3919dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807646 | ||||||
| chr12:55807646
|
C | CAA | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0219others(6): Show | 9 | HG00438.hp2 NA18981.hp2 NA19000.hp1 others(6): Show |
intron_variant | MODIFIER | c.37-3920_37-3919dup others(2): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807646 | ||||||
| chr12:55807813
|
C | CA | 15 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0001g0064others(12): Show | 15 | HG02027.hp1 HG02027.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-4086dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807813 | ||||||
| chr12:55807813
|
CA | C | 31 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0031others(28): Show | 31 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.37-4086delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807813 | ||||||
| chr12:55807832
|
A | T | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(28): Show | 31 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.37-4104T>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807832 | ||||||
| chr12:55807910
|
C | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 271 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.37-4182G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55807910 | ||||||
| chr12:55808100
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.37-4372A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808100 | ||||||
| chr12:55808124
|
T | C | 1 | a0001c0001t0002g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.37-4396A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808124 | ||||||
| chr12:55808270
|
GC | G | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG00741.hp1 HG02109.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-4543delG | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808270 | ||||||
| chr12:55808275
|
G | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-4547C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808275 | ||||||
| chr12:55808398
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.37-4670T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808398 | ||||||
| chr12:55808562
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.37-4834C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808562 | ||||||
| chr12:55808576
|
C | T | 49 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(46): Show | 49 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.37-4848G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808576 | ||||||
| chr12:55808672
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.37-4944C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808672 | ||||||
| chr12:55808833
|
AC | A | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.37-5106delG | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808833 | ||||||
| chr12:55808968
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.37-5240C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55808968 | ||||||
| chr12:55809004
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG00733.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.37-5276G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809004 | ||||||
| chr12:55809138
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.37-5410G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809138 | ||||||
| chr12:55809182
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.37-5454C>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809182 | ||||||
| chr12:55809281
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.37-5553A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809281 | ||||||
| chr12:55809581
|
C | T | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.37-5853G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809581 | ||||||
| chr12:55809611
|
G | GGCATGGT others(3): Show |
267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 271 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.37-5884_37-5883ins others(10): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809611 | ||||||
| chr12:55809627
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.37-5899A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809627 | ||||||
| chr12:55809655
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.37-5927T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809655 | ||||||
| chr12:55809674
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.37-5946A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809674 | ||||||
| chr12:55809721
|
C | T | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.37-5993G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809721 | ||||||
| chr12:55809750
|
C | CA | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 155 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.37-6023dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55809750 | ||||||
| chr12:55810061
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0199 | 2 | NA18975.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.37-6333A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810061 | ||||||
| chr12:55810179
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.37-6451G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810179 | ||||||
| chr12:55810262
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.37-6534C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810262 | ||||||
| chr12:55810451
|
A | AT | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-6724dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810451 | ||||||
| chr12:55810451
|
AT | A | 75 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(72): Show | 75 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.37-6724delA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810451 | ||||||
| chr12:55810521
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0002g0087 | 2 | NA18999.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.37-6793G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810521 | ||||||
| chr12:55810522
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.37-6794C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810522 | ||||||
| chr12:55810610
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.37-6882C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810610 | ||||||
| chr12:55810749
|
G | A | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(28): Show | 31 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.36+6917C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810749 | ||||||
| chr12:55810843
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.36+6823C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55810843 | ||||||
| chr12:55811081
|
CA | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(261): Show | 268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.36+6584delT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55811081 | ||||||
| chr12:55811142
|
T | G | 1 | a0001c0001t0002g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.36+6524A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55811142 | ||||||
| chr12:55811495
|
A | AG | 5 | a0001c0001t0001g0053a0001c0001t0003g0065a0001c0001t0003g0066others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+6170dupC | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55811495 | ||||||
| chr12:55811572
|
AAAAC | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.36+6090_36+6093del others(4): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55811572 | ||||||
| chr12:55811572
|
AAAACAAA others(1): Show |
A | 5 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0078others(2): Show | 5 | HG00733.hp2 HG02622.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+6086_36+6093del others(8): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55811572 | ||||||
| chr12:55811605
|
A | AAACC | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 140 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.36+6057_36+6060dup others(4): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55811605 | ||||||
| chr12:55811605
|
A | AAACCAAC others(1): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0105 | 3 | HG02622.hp1 HG03654.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.36+6060_36+6061ins others(8): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55811605 | ||||||
| chr12:55811901
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | NA18974.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.36+5765G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55811901 | ||||||
| chr12:55812195
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.36+5471A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812195 | ||||||
| chr12:55812282
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG00733.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.36+5384G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812282 | ||||||
| chr12:55812427
|
G | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 271 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.36+5239C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812427 | ||||||
| chr12:55812699
|
T | C | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.36+4967A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812699 | ||||||
| chr12:55812740
|
A | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.36+4926T>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812740 | ||||||
| chr12:55812784
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.36+4882A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812784 | ||||||
| chr12:55812830
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.36+4836T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812830 | ||||||
| chr12:55812877
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.36+4789T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812877 | ||||||
| chr12:55812897
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.36+4769C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812897 | ||||||
| chr12:55812940
|
A | G | 1 | a0001c0001t0001g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.36+4726T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55812940 | ||||||
| chr12:55813070
|
C | A | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.36+4596G>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813070 | ||||||
| chr12:55813273
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.36+4393C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813273 | ||||||
| chr12:55813277
|
T | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG00741.hp1 HG02109.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.36+4389A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813277 | ||||||
| chr12:55813308
|
T | C | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+4358A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813308 | ||||||
| chr12:55813419
|
G | A | 56 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0215others(53): Show | 56 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.36+4247C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813419 | ||||||
| chr12:55813539
|
A | AT | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 225 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.36+4126dupA | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813539 | ||||||
| chr12:55813539
|
A | ATT | 42 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(39): Show | 42 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.36+4125_36+4126dup others(2): Show |
SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813539 | ||||||
| chr12:55813613
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.36+4053G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813613 | ||||||
| chr12:55813709
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.36+3957A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55813709 | ||||||
| chr12:55814104
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.36+3562A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814104 | ||||||
| chr12:55814146
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.36+3520C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814146 | ||||||
| chr12:55814202
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.36+3464G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814202 | ||||||
| chr12:55814317
|
A | C | 1 | a0001c0001t0002g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36+3349T>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814317 | ||||||
| chr12:55814371
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+3295T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814371 | ||||||
| chr12:55814537
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.36+3129G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814537 | ||||||
| chr12:55814648
|
T | A | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.36+3018A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814648 | ||||||
| chr12:55814817
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.36+2849G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814817 | ||||||
| chr12:55814858
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA19064.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.36+2808C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814858 | ||||||
| chr12:55814873
|
T | TA | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.36+2792dupT | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814873 | ||||||
| chr12:55814900
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.36+2766T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814900 | ||||||
| chr12:55814954
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.36+2712T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814954 | ||||||
| chr12:55814996
|
T | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG00741.hp1 HG02109.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.36+2670A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55814996 | ||||||
| chr12:55815043
|
G | A | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.36+2623C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55815043 | ||||||
| chr12:55815232
|
A | G | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.36+2434T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55815232 | ||||||
| chr12:55815566
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.36+2100G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55815566 | ||||||
| chr12:55815608
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.36+2058G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55815608 | ||||||
| chr12:55815648
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.36+2018C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55815648 | ||||||
| chr12:55815803
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.36+1863C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55815803 | ||||||
| chr12:55816169
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0002g0087 | 2 | NA18999.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.36+1497G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55816169 | ||||||
| chr12:55816192
|
G | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 145 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.36+1474C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55816192 | ||||||
| chr12:55816318
|
A | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG02004.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.36+1348T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55816318 | ||||||
| chr12:55816647
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.36+1019A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55816647 | ||||||
| chr12:55816649
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.36+1017A>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55816649 | ||||||
| chr12:55816705
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.36+961G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55816705 | ||||||
| chr12:55816784
|
T | A | 54 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(51): Show | 54 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.36+882A>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55816784 | ||||||
| chr12:55816820
|
A | G | 1 | a0001c0001t0001g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+846T>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55816820 | ||||||
| chr12:55817111
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.36+555C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55817111 | ||||||
| chr12:55817125
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.36+541C>T | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55817125 | ||||||
| chr12:55817214
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.36+452A>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55817214 | ||||||
| chr12:55817248
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG02132.hp2 NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.36+418G>A | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55817248 | ||||||
| chr12:55817566
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.36+100C>G | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55817566 | ||||||
| chr12:55817653
|
C | G | 1 | a0001c0001t0002g0005 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.36+13G>C | SARNP | ENSG00000205323.9 | transcript | ENST00000336133.8 | protein_coding | 1/10 | chr12 | 55817653 |