Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4659 |
|---|---|
| ensemblid | ENSG00000058272.19 |
| hgncid | 7618 |
| symbol | PPP1R12A |
| name | protein phosphatase 1 regulatory subunit 12A |
| refseq_nuc | NM_002480.3 |
| refseq_prot | NP_002471.1 |
| ensembl_nuc | ENST00000450142.7 |
| ensembl_prot | ENSP00000389168.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 79773568 |
| end | 79935097 |
| strand | - |
| ver | v1.2 |
| region | chr12:79773568-79935097 |
| region5000 | chr12:79768568-79940097 |
| regionname0 | PPP1R12A_chr12_79773568_79935097 |
| regionname5000 | PPP1R12A_chr12_79768568_79940097 |
| 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 | 1030 | 307 | 73 | 40 | 149 | 8 | 35 | 111 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0002 | 0/0 | 1030 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0003 | 0/0 | 1030 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0004 | 0/0 | 1030 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0005 | 0/0 | 1030 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0006 | 0/0 | 1030 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| 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 | 3093 | 185 | 33 | 28 | 92 | 5 | 25 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| c0002 | 0/0 | 3093 | 120 | 39 | 12 | 56 | 3 | 10 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| c0003 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| c0004 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| c0005 | 0/0 | 3093 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| c0006 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| c0007 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| c0008 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| c0009 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2526 | 70 | 4 | 16 | 32 | 5 | 12 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0002 | 0/0 | 2528 | 56 | 0 | 4 | 44 | 0 | 8 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0003 | 0/0 | 2523 | 55 | 17 | 6 | 25 | 0 | 7 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0004 | 0/0 | 2526 | 43 | 2 | 6 | 30 | 0 | 5 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0005 | 0/0 | 2529 | 30 | 21 | 6 | 0 | 3 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0006 | 0/0 | 2527 | 19 | 4 | 0 | 13 | 0 | 2 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0007 | 0/0 | 2522 | 10 | 10 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0008 | 0/0 | 2529 | 7 | 6 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0009 | 0/0 | 2526 | 7 | 6 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0010 | 0/0 | 2526 | 4 | 4 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0011 | 0/0 | 2523 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0012 | 0/0 | 2523 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0013 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0014 | 0/0 | 2524 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0015 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0016 | 0/0 | 2527 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0017 | 1/0 | 2528 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0018 | 0/0 | 2526 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0019 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| t0020 | 0/0 | 2526 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| 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 | 3093 | 185 | 33 | 28 | 92 | 5 | 25 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0002 | 0/0 | 3093 | 120 | 39 | 12 | 56 | 3 | 10 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0003 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0006 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0002c0009 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0003c0008 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0004c0004 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0005c0005 | 0/0 | 3093 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0006c0007 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5618 | 70 | 4 | 16 | 32 | 5 | 12 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0003 | 0/0 | 5615 | 53 | 17 | 6 | 24 | 0 | 6 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0004 | 0/0 | 5618 | 43 | 2 | 6 | 30 | 0 | 5 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0007 | 0/0 | 5614 | 10 | 10 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0011 | 0/0 | 5615 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0012 | 0/0 | 5615 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0014 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0016 | 0/0 | 5619 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0017 | 1/0 | 5620 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0018 | 0/0 | 5618 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0019 | 0/0 | 5632 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0001t0020 | 0/0 | 5618 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0002t0002 | 0/0 | 5620 | 55 | 0 | 4 | 43 | 0 | 8 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0002t0005 | 0/0 | 5621 | 28 | 19 | 6 | 0 | 3 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0002t0006 | 0/0 | 5619 | 19 | 4 | 0 | 13 | 0 | 2 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0002t0008 | 0/0 | 5621 | 7 | 6 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0002t0009 | 0/0 | 5618 | 6 | 5 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0002t0010 | 0/0 | 5618 | 4 | 4 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0002t0013 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0003t0015 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0001c0006t0002 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0002c0009t0005 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0003c0008t0003 | 0/0 | 5615 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0004c0004t0005 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0005c0005t0003 | 0/0 | 5615 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| a0006c0007t0009 | 0/0 | 5618 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | copy fasta | chr12 | 79768568 | 79940097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0011g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0011g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0014g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0016g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0017g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0018g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0019g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0001t0020g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0008g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0009g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0010g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0002t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0003t0015g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0001c0006t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0002c0009t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0003c0008t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0004c0004t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0005c0005t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| a0006c0007t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00140 | hp2 | a0001 | c0002 | t0005 | g0114 | EUR | GBR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00673 | hp2 | a0001 | c0006 | t0002 | g0016 | EAS | CHS | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01074 | hp2 | a0001 | c0002 | t0009 | g0093 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0042 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0113 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01168 | hp1 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0003 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01192 | hp2 | a0001 | c0002 | t0005 | g0111 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01243 | hp1 | a0001 | c0002 | t0008 | g0097 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0103 | AMR | CLM | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0112 | AMR | CLM | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0298 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0303 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0271 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0299 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0139 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02055 | hp2 | a0001 | c0002 | t0010 | g0007 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02145 | hp1 | a0001 | c0002 | t0005 | g0125 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02145 | hp2 | a0001 | c0003 | t0015 | g0086 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0290 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | CDX | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | CDX | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0099 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0136 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02258 | hp1 | a0001 | c0002 | t0009 | g0094 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02258 | hp2 | a0001 | c0002 | t0005 | g0122 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02280 | hp1 | a0001 | c0002 | t0008 | g0088 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02280 | hp2 | a0002 | c0009 | t0005 | g0118 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0286 | AMR | PEL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02451 | hp1 | a0001 | c0002 | t0008 | g0090 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0143 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0123 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0141 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0121 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0013 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02717 | hp1 | a0004 | c0004 | t0005 | g0117 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0108 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0104 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0098 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02886 | hp2 | a0001 | c0002 | t0006 | g0037 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02896 | hp2 | a0001 | c0002 | t0008 | g0096 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0124 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0101 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0140 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02970 | hp2 | a0001 | c0002 | t0010 | g0009 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02976 | hp1 | a0001 | c0002 | t0010 | g0008 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0105 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03041 | hp2 | a0001 | c0002 | t0009 | g0012 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03130 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03130 | hp2 | a0001 | c0002 | t0013 | g0089 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03195 | hp2 | a0001 | c0002 | t0005 | g0102 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0119 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03225 | hp2 | a0001 | c0002 | t0008 | g0095 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0291 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03453 | hp1 | a0001 | c0002 | t0010 | g0265 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03453 | hp2 | a0001 | c0002 | t0005 | g0107 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0193 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0277 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0062 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0106 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ESN | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03540 | hp1 | a0001 | c0002 | t0005 | g0120 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | MSL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03710 | hp2 | a0001 | c0002 | t0006 | g0033 | SAS | PJL | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03831 | hp1 | a0001 | c0002 | t0006 | g0079 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0279 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0063 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04115 | hp1 | a0001 | c0001 | t0012 | g0167 | SAS | STU | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0309 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0227 | SAS | BEB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04199 | hp1 | a0005 | c0005 | t0003 | g0185 | SAS | STU | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | STU | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | STU | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0297 | SAS | STU | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0054 | SAS | STU | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18522 | hp1 | a0001 | c0002 | t0009 | g0011 | AFR | YRI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18522 | hp2 | a0001 | c0002 | t0008 | g0087 | AFR | YRI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | CHB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | YRI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18906 | hp2 | a0006 | c0007 | t0009 | g0091 | AFR | YRI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18939 | hp1 | a0001 | c0002 | t0006 | g0083 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18942 | hp2 | a0001 | c0002 | t0006 | g0014 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18950 | hp1 | a0001 | c0001 | t0011 | g0304 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18953 | hp1 | a0001 | c0001 | t0019 | g0272 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18960 | hp1 | a0001 | c0001 | t0011 | g0302 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18961 | hp1 | a0001 | c0002 | t0006 | g0084 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18961 | hp2 | a0001 | c0001 | t0020 | g0310 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18968 | hp2 | a0001 | c0002 | t0006 | g0085 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18981 | hp1 | a0001 | c0002 | t0006 | g0076 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18988 | hp1 | a0001 | c0002 | t0006 | g0030 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18990 | hp2 | a0001 | c0002 | t0006 | g0080 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19030 | hp2 | a0001 | c0002 | t0005 | g0109 | AFR | LWK | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0137 | AFR | LWK | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19043 | hp2 | a0001 | c0002 | t0009 | g0092 | AFR | LWK | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19056 | hp1 | a0001 | c0002 | t0006 | g0077 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19060 | hp1 | a0001 | c0002 | t0006 | g0082 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19063 | hp2 | a0001 | c0002 | t0006 | g0081 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19070 | hp2 | a0001 | c0002 | t0006 | g0078 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19079 | hp2 | a0001 | c0001 | t0018 | g0266 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19082 | hp1 | a0001 | c0002 | t0006 | g0029 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19086 | hp2 | a0001 | c0002 | t0006 | g0075 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19089 | hp2 | a0001 | c0001 | t0014 | g0163 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19090 | hp1 | a0003 | c0008 | t0003 | g0131 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0110 | AFR | YRI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | YRI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA20752 | hp2 | a0001 | c0002 | t0005 | g0116 | EUR | TSI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA20805 | hp1 | a0001 | c0002 | t0005 | g0115 | EUR | TSI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0142 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02109 | hp2 | a0001 | c0002 | t0006 | g0034 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02486 | hp1 | a0001 | c0002 | t0006 | g0005 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0138 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0307 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG02559 | hp2 | a0001 | c0002 | t0009 | g0010 | AFR | ACB | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | USA | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| HG06807 | hp2 | a0001 | c0002 | t0005 | g0100 | AFR | USA | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0203 | REF | REF | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0017 | g0026 | REF | REF | PPP1R12A_chr12_79768568_79940097 | PPP1R12A | chr12 | 79768568 | 79940097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:79795759
|
T | C | 1 | a0005 | 1 | HG04199.hp1 | missense_variant&splice_region_variant | MODERATE | c.2462A>G | p.Glu821Gly | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/25 | 2628/5620 | 2462/3093 | 821/1030 | chr12 | 79795759 | ||
| chr12:79805608
|
C | T | 1 | a0004 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1984G>A | p.Val662Ile | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/25 | 2150/5620 | 1984/3093 | 662/1030 | chr12 | 79805608 | ||
| chr12:79805698
|
T | C | 1 | a0006 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1894A>G | p.Ile632Val | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/25 | 2060/5620 | 1894/3093 | 632/1030 | chr12 | 79805698 | ||
| chr12:79806328
|
G | A | 1 | a0003 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.1661C>T | p.Ser554Phe | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 13/25 | 1827/5620 | 1661/3093 | 554/1030 | chr12 | 79806328 | ||
| chr12:79807239
|
T | C | 1 | a0002 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1642A>G | p.Thr548Ala | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/25 | 1808/5620 | 1642/3093 | 548/1030 | chr12 | 79807239 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:79796870
|
C | G | 6 | a0001c0002a0001c0003a0001c0006others(3): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
synonymous_variant | LOW | c.2373G>C | p.Leu791Leu | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 17/25 | 2539/5620 | 2373/3093 | 791/1030 | chr12 | 79796870 | ||
| chr12:79798500
|
T | C | 1 | a0001c0006 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.2085A>G | p.Ser695Ser | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 15/25 | 2251/5620 | 2085/3093 | 695/1030 | chr12 | 79798500 | ||
| chr12:79820838
|
C | T | 1 | a0001c0003 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1050G>A | p.Lys350Lys | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/25 | 1216/5620 | 1050/3093 | 350/1030 | chr12 | 79820838 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:79773581
|
C | G | 3 | a0001c0002t0005a0002c0009t0005a0004c0004t0005 | 30 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2348G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 2348 | chr12 | 79773581 | |||||
| chr12:79774634
|
TA | T | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | 225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*1294delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 1294 | chr12 | 79774634 | |||||
| chr12:79774634
|
TAA | T | 1 | a0001c0001t0007 | 10 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1293_*1294delTT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 1293 | chr12 | 79774634 | |||||
| chr12:79774681
|
ATGG | A | 7 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(4): Show | 69 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1247delCCA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 1245 | chr12 | 79774681 | |||||
| chr12:79774864
|
G | C | 1 | a0001c0001t0020 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1065C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 1065 | chr12 | 79774864 | |||||
| chr12:79774880
|
G | A | 12 | a0001c0002t0002a0001c0002t0005a0001c0002t0006others(9): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1049C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 1049 | chr12 | 79774880 | |||||
| chr12:79774926
|
A | AGAT | 6 | a0001c0002t0005a0001c0002t0008a0001c0002t0013others(3): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1000_*1002dupATC | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 1002 | chr12 | 79774926 | |||||
| chr12:79775215
|
T | A | 1 | a0001c0003t0015 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*714A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 714 | chr12 | 79775215 | |||||
| chr12:79775306
|
T | C | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 623 | chr12 | 79775306 | |||||
| chr12:79775309
|
A | ACCTGGAA others(7): Show |
1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619_*620insAATTCA others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 619 | chr12 | 79775309 | |||||
| chr12:79775311
|
G | C | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*618C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 618 | chr12 | 79775311 | |||||
| chr12:79775313
|
G | T | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*616C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 616 | chr12 | 79775313 | |||||
| chr12:79775316
|
A | T | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 613 | chr12 | 79775316 | |||||
| chr12:79775318
|
A | G | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 611 | chr12 | 79775318 | |||||
| chr12:79775346
|
A | T | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 583 | chr12 | 79775346 | |||||
| chr12:79775349
|
A | G | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 580 | chr12 | 79775349 | |||||
| chr12:79775351
|
T | G | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 578 | chr12 | 79775351 | |||||
| chr12:79775356
|
G | T | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 573 | chr12 | 79775356 | |||||
| chr12:79775370
|
C | A | 1 | a0001c0002t0010 | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*559G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 559 | chr12 | 79775370 | |||||
| chr12:79775370
|
C | T | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*559G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 559 | chr12 | 79775370 | |||||
| chr12:79775371
|
T | C | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 558 | chr12 | 79775371 | |||||
| chr12:79775377
|
G | T | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 552 | chr12 | 79775377 | |||||
| chr12:79775378
|
T | A | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*551A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 551 | chr12 | 79775378 | |||||
| chr12:79775379
|
A | T | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*550T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 550 | chr12 | 79775379 | |||||
| chr12:79775394
|
A | T | 1 | a0001c0001t0019 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*535T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 535 | chr12 | 79775394 | |||||
| chr12:79775450
|
A | T | 1 | a0001c0002t0013 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*479T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 479 | chr12 | 79775450 | |||||
| chr12:79775664
|
A | G | 1 | a0001c0001t0012 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*265T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 265 | chr12 | 79775664 | |||||
| chr12:79775717
|
TA | T | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | 254 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*211delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 25/25 | 211 | chr12 | 79775717 | |||||
| chr12:79935060
|
A | C | 1 | a0001c0001t0018 | 1 | NA19079.hp2 | 5_prime_UTR_variant | MODIFIER | c.-129T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/25 | 129 | chr12 | 79935060 | |||||
| chr12:79935067
|
G | A | 5 | a0001c0001t0004a0001c0001t0011a0001c0001t0018others(2): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-136C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/25 | 136 | chr12 | 79935067 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:79776047
|
A | G | 1 | a0001c0002t0005g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3007-32T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79776047 | ||||||
| chr12:79776416
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3007-401A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79776416 | ||||||
| chr12:79776485
|
A | G | 2 | a0001c0002t0005g0106a0001c0002t0005g0111 | 2 | HG01192.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3007-470T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79776485 | ||||||
| chr12:79777156
|
TATTA | T | 124 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(121): Show | 124 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.3007-1145_3007-114 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777156 | ||||||
| chr12:79777252
|
G | C | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3007-1237C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777252 | ||||||
| chr12:79777412
|
C | G | 1 | a0001c0002t0002g0050 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3006+1138G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777412 | ||||||
| chr12:79777446
|
T | G | 1 | a0001c0001t0004g0286 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3006+1104A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777446 | ||||||
| chr12:79777521
|
T | C | 2 | a0001c0002t0006g0080a0001c0002t0006g0083 | 2 | NA18939.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.3006+1029A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777521 | ||||||
| chr12:79777532
|
A | T | 1 | a0001c0002t0002g0015 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3006+1018T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777532 | ||||||
| chr12:79777692
|
A | C | 1 | a0001c0002t0005g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3006+858T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777692 | ||||||
| chr12:79777739
|
T | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3006+811A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777739 | ||||||
| chr12:79777740
|
T | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3006+810A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777740 | ||||||
| chr12:79777741
|
A | T | 12 | a0001c0002t0002g0043a0001c0002t0002g0045a0001c0002t0002g0047others(9): Show | 12 | HG02027.hp1 NA18747.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.3006+809T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777741 | ||||||
| chr12:79777940
|
G | A | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.3006+610C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777940 | ||||||
| chr12:79777950
|
T | C | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.3006+600A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777950 | ||||||
| chr12:79777984
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3006+566A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79777984 | ||||||
| chr12:79778133
|
A | C | 1 | a0001c0002t0005g0124 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3006+417T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79778133 | ||||||
| chr12:79778200
|
A | C | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3006+350T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79778200 | ||||||
| chr12:79778213
|
GAATA | G | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.3006+333_3006+336d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79778213 | ||||||
| chr12:79778308
|
CGG | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3006+240_3006+241d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79778308 | ||||||
| chr12:79778340
|
T | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3006+210A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79778340 | ||||||
| chr12:79778513
|
A | T | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3006+37T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 24/24 | chr12 | 79778513 | ||||||
| chr12:79778847
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2956-247T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79778847 | ||||||
| chr12:79778880
|
A | G | 1 | a0001c0001t0004g0309 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2956-280T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79778880 | ||||||
| chr12:79778881
|
G | C | 9 | a0001c0001t0001g0241a0001c0001t0004g0001a0001c0001t0004g0273others(6): Show | 10 | HG00673.hp1 NA18956.hp1 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.2956-281C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79778881 | ||||||
| chr12:79778917
|
G | A | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.2956-317C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79778917 | ||||||
| chr12:79779079
|
A | G | 3 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0013g0089 | 3 | HG02280.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2956-479T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79779079 | ||||||
| chr12:79779158
|
G | A | 1 | a0001c0001t0003g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2956-558C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79779158 | ||||||
| chr12:79780119
|
G | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2956-1519C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780119 | ||||||
| chr12:79780152
|
G | A | 1 | a0001c0002t0009g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2956-1552C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780152 | ||||||
| chr12:79780216
|
GACAA | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG01934.hp1 HG01943.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.2955+1595_2955+159 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780216 | ||||||
| chr12:79780226
|
C | CA | 37 | a0001c0001t0001g0241a0001c0001t0004g0001a0001c0001t0004g0268others(34): Show | 38 | HG00408.hp1 HG00673.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.2955+1588dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780226 | ||||||
| chr12:79780230
|
A | C | 3 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0013g0089 | 3 | HG02280.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2955+1585T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780230 | ||||||
| chr12:79780391
|
T | C | 1 | a0001c0001t0004g0299 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2955+1424A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780391 | ||||||
| chr12:79780420
|
G | A | 3 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009 | 3 | HG02055.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2955+1395C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780420 | ||||||
| chr12:79780450
|
T | A | 1 | a0001c0001t0003g0169 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2955+1365A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780450 | ||||||
| chr12:79780457
|
G | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2955+1358C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780457 | ||||||
| chr12:79780537
|
A | C | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2955+1278T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780537 | ||||||
| chr12:79780658
|
G | A | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2955+1157C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780658 | ||||||
| chr12:79780940
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2955+875C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780940 | ||||||
| chr12:79780994
|
C | T | 4 | a0001c0002t0005g0119a0001c0002t0005g0120a0001c0002t0005g0121others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+821G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79780994 | ||||||
| chr12:79781129
|
G | A | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2955+686C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79781129 | ||||||
| chr12:79781225
|
C | G | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2955+590G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79781225 | ||||||
| chr12:79781356
|
TATTAA | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+454_2955+458d others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79781356 | ||||||
| chr12:79781504
|
A | G | 1 | a0001c0002t0002g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2955+311T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79781504 | ||||||
| chr12:79781542
|
G | A | 1 | a0001c0002t0002g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2955+273C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79781542 | ||||||
| chr12:79781800
|
A | T | 1 | a0001c0001t0003g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2955+15T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 23/24 | chr12 | 79781800 | ||||||
| chr12:79781984
|
G | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2908-122C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79781984 | ||||||
| chr12:79781993
|
A | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2908-131T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79781993 | ||||||
| chr12:79782117
|
T | C | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2908-255A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79782117 | ||||||
| chr12:79782185
|
C | G | 1 | a0001c0001t0001g0260 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2908-323G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79782185 | ||||||
| chr12:79782554
|
C | T | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2908-692G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79782554 | ||||||
| chr12:79782658
|
C | G | 1 | a0001c0002t0013g0089 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2908-796G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79782658 | ||||||
| chr12:79782861
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2908-999T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79782861 | ||||||
| chr12:79782876
|
A | C | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2908-1014T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79782876 | ||||||
| chr12:79782904
|
T | A | 1 | a0001c0001t0003g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2908-1042A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79782904 | ||||||
| chr12:79783193
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2908-1331A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783193 | ||||||
| chr12:79783258
|
G | C | 1 | a0001c0002t0006g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2908-1396C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783258 | ||||||
| chr12:79783295
|
C | CA | 186 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(183): Show | 187 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.2908-1434dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783295 | ||||||
| chr12:79783295
|
C | CAA | 23 | a0001c0001t0001g0233a0001c0001t0001g0241a0001c0001t0001g0253others(20): Show | 23 | HG01243.hp1 HG01496.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.2908-1435_2908-143 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783295 | ||||||
| chr12:79783295
|
C | CAAA | 19 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0100others(16): Show | 19 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.2908-1436_2908-143 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783295 | ||||||
| chr12:79783295
|
C | CAAAA | 6 | a0001c0002t0005g0099a0001c0002t0005g0106a0001c0002t0005g0111others(3): Show | 6 | HG01192.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2908-1437_2908-143 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783295 | ||||||
| chr12:79783455
|
G | A | 1 | a0001c0002t0002g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2908-1593C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783455 | ||||||
| chr12:79783506
|
C | T | 308 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(305): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.2908-1644G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783506 | ||||||
| chr12:79783781
|
A | G | 1 | a0001c0001t0004g0292 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2908-1919T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79783781 | ||||||
| chr12:79784128
|
T | C | 1 | a0001c0002t0005g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2907+2246A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784128 | ||||||
| chr12:79784289
|
A | G | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2907+2085T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784289 | ||||||
| chr12:79784466
|
C | T | 2 | a0001c0001t0004g0274a0001c0001t0004g0288 | 2 | NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2907+1908G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784466 | ||||||
| chr12:79784631
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2907+1743C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784631 | ||||||
| chr12:79784693
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2907+1681T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784693 | ||||||
| chr12:79784781
|
C | T | 11 | a0001c0001t0001g0196a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG00323.hp1 HG00639.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.2907+1593G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784781 | ||||||
| chr12:79784808
|
T | C | 3 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009 | 3 | HG02055.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2907+1566A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784808 | ||||||
| chr12:79784858
|
C | T | 1 | a0001c0001t0004g0282 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2907+1516G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784858 | ||||||
| chr12:79784894
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2907+1480G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784894 | ||||||
| chr12:79784907
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2907+1467C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79784907 | ||||||
| chr12:79785402
|
A | C | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2907+972T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79785402 | ||||||
| chr12:79785576
|
G | T | 1 | a0001c0001t0004g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2907+798C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79785576 | ||||||
| chr12:79785612
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2907+762C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79785612 | ||||||
| chr12:79785998
|
C | G | 47 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.2907+376G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79785998 | ||||||
| chr12:79786161
|
T | C | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2907+213A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79786161 | ||||||
| chr12:79786290
|
A | T | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2907+84T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 22/24 | chr12 | 79786290 | ||||||
| chr12:79786640
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2803-162C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79786640 | ||||||
| chr12:79786698
|
T | C | 2 | a0001c0002t0002g0025a0001c0002t0002g0028 | 2 | HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2803-220A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79786698 | ||||||
| chr12:79786923
|
T | C | 3 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0013g0089 | 3 | HG02280.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2803-445A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79786923 | ||||||
| chr12:79786946
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2803-468G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79786946 | ||||||
| chr12:79787025
|
C | T | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2803-547G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79787025 | ||||||
| chr12:79787098
|
C | G | 2 | a0001c0001t0004g0282a0001c0001t0018g0266 | 2 | NA18990.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2803-620G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79787098 | ||||||
| chr12:79787199
|
C | T | 70 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.2803-721G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79787199 | ||||||
| chr12:79787249
|
C | T | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2803-771G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79787249 | ||||||
| chr12:79787250
|
G | A | 22 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0202others(19): Show | 22 | HG00323.hp2 HG00438.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2803-772C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79787250 | ||||||
| chr12:79787573
|
G | A | 7 | a0001c0001t0004g0280a0001c0001t0004g0281a0001c0001t0020g0310others(4): Show | 7 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2802+1075C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79787573 | ||||||
| chr12:79787663
|
C | T | 7 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0112others(4): Show | 7 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.2802+985G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79787663 | ||||||
| chr12:79788057
|
G | A | 1 | a0001c0002t0002g0074 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2802+591C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79788057 | ||||||
| chr12:79788194
|
A | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2802+454T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79788194 | ||||||
| chr12:79788565
|
A | G | 1 | a0001c0001t0007g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2802+83T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79788565 | ||||||
| chr12:79788632
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2802+16A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 21/24 | chr12 | 79788632 | ||||||
| chr12:79789342
|
C | T | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.2667-559G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 20/24 | chr12 | 79789342 | ||||||
| chr12:79789410
|
A | G | 1 | a0005c0005t0003g0185 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2667-627T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 20/24 | chr12 | 79789410 | ||||||
| chr12:79789489
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2667-706T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 20/24 | chr12 | 79789489 | ||||||
| chr12:79789778
|
CT | C | 177 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(174): Show | 178 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2666+688delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 20/24 | chr12 | 79789778 | ||||||
| chr12:79789778
|
CTT | C | 6 | a0001c0001t0001g0218a0001c0001t0001g0226a0001c0001t0001g0238others(3): Show | 6 | HG00639.hp2 HG01975.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2666+687_2666+688d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 20/24 | chr12 | 79789778 | ||||||
| chr12:79789952
|
A | T | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2666+515T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 20/24 | chr12 | 79789952 | ||||||
| chr12:79789954
|
A | AT | 6 | a0001c0001t0004g0277a0001c0001t0007g0140a0001c0002t0005g0122others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2666+512dupA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 20/24 | chr12 | 79789954 | ||||||
| chr12:79789971
|
T | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2666+496A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 20/24 | chr12 | 79789971 | ||||||
| chr12:79790806
|
T | C | 1 | a0001c0002t0002g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2650-323A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79790806 | ||||||
| chr12:79790831
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2650-348C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79790831 | ||||||
| chr12:79791065
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0016g0227 | 2 | HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2650-582A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79791065 | ||||||
| chr12:79791172
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2650-689G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79791172 | ||||||
| chr12:79791599
|
C | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2650-1116G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79791599 | ||||||
| chr12:79791670
|
G | A | 2 | a0001c0001t0001g0228a0001c0002t0005g0125 | 2 | HG01074.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2650-1187C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79791670 | ||||||
| chr12:79791791
|
A | G | 1 | a0001c0002t0005g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2650-1308T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79791791 | ||||||
| chr12:79791878
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2650-1395T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79791878 | ||||||
| chr12:79791936
|
C | T | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.2650-1453G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79791936 | ||||||
| chr12:79791974
|
G | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2650-1491C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79791974 | ||||||
| chr12:79792063
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2650-1580G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79792063 | ||||||
| chr12:79792132
|
C | A | 7 | a0001c0002t0006g0075a0001c0002t0006g0080a0001c0002t0006g0081others(4): Show | 7 | NA18939.hp1 NA18961.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.2650-1649G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79792132 | ||||||
| chr12:79792175
|
T | C | 2 | a0001c0001t0003g0171a0001c0001t0003g0172 | 2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.2649+1688A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79792175 | ||||||
| chr12:79792285
|
T | C | 34 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0177others(31): Show | 34 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.2649+1578A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79792285 | ||||||
| chr12:79792564
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2649+1299T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79792564 | ||||||
| chr12:79792605
|
G | C | 34 | a0001c0001t0001g0241a0001c0001t0004g0001a0001c0001t0004g0268others(31): Show | 35 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2649+1258C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79792605 | ||||||
| chr12:79792656
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2649+1207A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79792656 | ||||||
| chr12:79792682
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2649+1181G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79792682 | ||||||
| chr12:79793349
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2649+514A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79793349 | ||||||
| chr12:79793799
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2649+64C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 19/24 | chr12 | 79793799 | ||||||
| chr12:79794007
|
G | A | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2584-79C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79794007 | ||||||
| chr12:79794032
|
T | C | 5 | a0001c0002t0005g0105a0001c0002t0005g0107a0001c0002t0005g0108others(2): Show | 5 | HG02809.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2584-104A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79794032 | ||||||
| chr12:79794580
|
T | TA | 6 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0113others(3): Show | 6 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2584-653dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79794580 | ||||||
| chr12:79794764
|
GAATA | G | 70 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.2584-840_2584-837d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79794764 | ||||||
| chr12:79794815
|
T | G | 1 | a0001c0001t0003g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2583+823A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79794815 | ||||||
| chr12:79795021
|
T | C | 7 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(4): Show | 7 | HG00438.hp2 HG03834.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.2583+617A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79795021 | ||||||
| chr12:79795061
|
C | T | 70 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.2583+577G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79795061 | ||||||
| chr12:79795515
|
CA | C | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2583+122delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79795515 | ||||||
| chr12:79795554
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2583+84T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79795554 | ||||||
| chr12:79795564
|
T | C | 22 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0202others(19): Show | 22 | HG00323.hp2 HG00438.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2583+74A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 18/24 | chr12 | 79795564 | ||||||
| chr12:79796260
|
GAA | G | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2462-503_2462-502d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 17/24 | chr12 | 79796260 | ||||||
| chr12:79796556
|
A | G | 2 | a0001c0001t0004g0282a0001c0001t0018g0266 | 2 | NA18990.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2461+226T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 17/24 | chr12 | 79796556 | ||||||
| chr12:79796612
|
A | G | 1 | a0004c0004t0005g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2461+170T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 17/24 | chr12 | 79796612 | ||||||
| chr12:79796676
|
A | G | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2461+106T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 17/24 | chr12 | 79796676 | ||||||
| chr12:79797425
|
T | C | 1 | a0001c0001t0018g0266 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2092-30A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 15/24 | chr12 | 79797425 | ||||||
| chr12:79797453
|
A | C | 2 | a0001c0001t0004g0268a0001c0001t0004g0269 | 2 | HG00408.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.2092-58T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 15/24 | chr12 | 79797453 | ||||||
| chr12:79797581
|
G | A | 1 | a0001c0002t0006g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2092-186C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 15/24 | chr12 | 79797581 | ||||||
| chr12:79797697
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0205a0001c0001t0001g0233 | 3 | HG02723.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2092-302C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 15/24 | chr12 | 79797697 | ||||||
| chr12:79797707
|
A | G | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2092-312T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 15/24 | chr12 | 79797707 | ||||||
| chr12:79798033
|
C | T | 186 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(183): Show | 187 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.2091+461G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 15/24 | chr12 | 79798033 | ||||||
| chr12:79798322
|
G | C | 1 | a0001c0001t0003g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2091+172C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 15/24 | chr12 | 79798322 | ||||||
| chr12:79798860
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2001-276G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79798860 | ||||||
| chr12:79799201
|
T | A | 1 | a0001c0002t0006g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2001-617A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79799201 | ||||||
| chr12:79799209
|
C | T | 1 | a0001c0002t0006g0014 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2001-625G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79799209 | ||||||
| chr12:79799309
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001-725G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79799309 | ||||||
| chr12:79799434
|
G | A | 4 | a0001c0002t0005g0105a0001c0002t0005g0107a0001c0002t0005g0108others(1): Show | 4 | HG02809.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-850C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79799434 | ||||||
| chr12:79799581
|
T | C | 240 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0003g0006others(237): Show | 241 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.2001-997A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79799581 | ||||||
| chr12:79799677
|
C | T | 1 | a0001c0002t0008g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2001-1093G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79799677 | ||||||
| chr12:79799840
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2001-1256G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79799840 | ||||||
| chr12:79799904
|
G | A | 1 | a0001c0002t0005g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2001-1320C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79799904 | ||||||
| chr12:79800117
|
C | T | 1 | a0001c0002t0002g0024 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2001-1533G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800117 | ||||||
| chr12:79800121
|
T | C | 49 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(46): Show | 50 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.2001-1537A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800121 | ||||||
| chr12:79800355
|
G | A | 240 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0003g0006others(237): Show | 241 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.2001-1771C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800355 | ||||||
| chr12:79800386
|
A | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2001-1802T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800386 | ||||||
| chr12:79800390
|
TCTTC | T | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001-1810_2001-180 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800390 | ||||||
| chr12:79800628
|
G | A | 1 | a0002c0009t0005g0118 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2001-2044C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800628 | ||||||
| chr12:79800733
|
CT | C | 72 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0201others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2001-2150delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800733 | ||||||
| chr12:79800879
|
G | A | 1 | a0001c0001t0003g0133 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2001-2295C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800879 | ||||||
| chr12:79800890
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2001-2306G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800890 | ||||||
| chr12:79800934
|
C | A | 1 | a0001c0002t0008g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2001-2350G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79800934 | ||||||
| chr12:79801024
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2001-2440A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801024 | ||||||
| chr12:79801072
|
G | A | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2001-2488C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801072 | ||||||
| chr12:79801120
|
C | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2001-2536G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801120 | ||||||
| chr12:79801236
|
TCAGGAGG others(6): Show |
T | 120 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2001-2665_2001-265 others(17): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801236 | ||||||
| chr12:79801345
|
C | CA | 15 | a0001c0001t0001g0196a0001c0001t0001g0219a0001c0001t0001g0222others(12): Show | 15 | HG00323.hp1 HG01168.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.2001-2762dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAA | 8 | a0001c0001t0001g0233a0001c0001t0001g0255a0001c0001t0001g0256others(5): Show | 8 | HG01261.hp1 HG02818.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.2001-2764_2001-276 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0202a0001c0001t0003g0184 | 2 | HG03942.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2001-2771_2001-276 others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0003g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2001-2772_2001-276 others(15): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2001-2773_2001-276 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0003g0179a0001c0002t0005g0101 | 2 | HG02965.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2001-2774_2001-276 others(17): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0003g0173a0001c0001t0003g0176a0001c0001t0003g0186 | 3 | NA18969.hp1 NA18986.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2001-2775_2001-276 others(18): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(8): Show |
1 | a0003c0008t0003g0131 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2001-2776_2001-276 others(19): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0207 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2001-2777_2001-276 others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0003g0006a0001c0001t0011g0302 | 2 | NA18960.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2001-2779_2001-276 others(22): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0209a0001c0001t0014g0163 | 2 | HG04204.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2001-2780_2001-276 others(23): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0003g0133a0001c0001t0003g0189 | 2 | NA19062.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2001-2781_2001-276 others(24): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0003g0162a0001c0001t0003g0175 | 2 | HG00408.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2001-2782_2001-276 others(25): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0003g0171 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2001-2786_2001-276 others(29): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0003g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2001-2787_2001-276 others(30): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CA | C | 28 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0198others(25): Show | 28 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2001-2762delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAA | C | 7 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0160others(4): Show | 7 | HG01109.hp2 HG01168.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-2766_2001-276 others(9): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0003g0180a0001c0001t0003g0182a0001c0001t0007g0134others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-2770_2001-276 others(13): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0003g0158a0001c0001t0007g0138 | 2 | HG02083.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2001-2771_2001-276 others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2001-2772_2001-276 others(15): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0003g0145a0001c0001t0003g0148a0001c0001t0003g0151others(2): Show | 5 | HG02622.hp1 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2001-2773_2001-276 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(6): Show |
C | 21 | a0001c0001t0001g0250a0001c0001t0003g0128a0001c0001t0003g0132others(18): Show | 21 | HG00438.hp2 HG00639.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.2001-2774_2001-276 others(17): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(7): Show |
C | 71 | a0001c0001t0003g0169a0001c0001t0012g0167a0001c0002t0002g0004others(68): Show | 71 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.2001-2775_2001-276 others(18): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0002t0002g0015a0001c0002t0005g0124a0001c0002t0009g0092others(1): Show | 4 | HG01074.hp2 HG02040.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001-2776_2001-276 others(19): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0003g0187a0001c0002t0009g0010a0001c0002t0009g0011others(1): Show | 4 | HG00544.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-2777_2001-276 others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0220a0001c0001t0001g0261 | 2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2001-2778_2001-276 others(21): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(11): Show |
C | 5 | a0001c0001t0004g0267a0001c0002t0008g0095a0001c0002t0008g0096others(2): Show | 5 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2001-2779_2001-276 others(22): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(12): Show |
C | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-2780_2001-276 others(23): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(13): Show |
C | 4 | a0001c0002t0002g0061a0001c0002t0005g0106a0001c0002t0005g0110others(1): Show | 4 | HG01192.hp2 HG03516.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-2781_2001-276 others(24): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(16): Show |
C | 35 | a0001c0001t0001g0241a0001c0001t0004g0001a0001c0001t0004g0268others(32): Show | 36 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.2001-2784_2001-276 others(27): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(17): Show |
C | 11 | a0001c0001t0001g0130a0001c0001t0004g0298a0001c0001t0004g0299others(8): Show | 11 | HG01928.hp1 HG02015.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.2001-2785_2001-276 others(28): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801345
|
CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0003g0164 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2001-2786_2001-276 others(29): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801345 | ||||||
| chr12:79801387
|
C | G | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2001-2803G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801387 | ||||||
| chr12:79801542
|
G | A | 254 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(251): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2001-2958C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801542 | ||||||
| chr12:79801701
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2001-3117T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801701 | ||||||
| chr12:79801727
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2001-3143G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801727 | ||||||
| chr12:79801752
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2001-3168G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801752 | ||||||
| chr12:79801913
|
C | T | 10 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2001-3329G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79801913 | ||||||
| chr12:79802194
|
A | G | 1 | a0001c0002t0002g0069 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2000+3398T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79802194 | ||||||
| chr12:79802222
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2000+3370G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79802222 | ||||||
| chr12:79802537
|
C | T | 1 | a0001c0001t0003g0176 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2000+3055G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79802537 | ||||||
| chr12:79802538
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2000+3054C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79802538 | ||||||
| chr12:79802644
|
G | A | 1 | a0001c0002t0006g0014 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2000+2948C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79802644 | ||||||
| chr12:79802897
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2000+2695A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79802897 | ||||||
| chr12:79802970
|
T | C | 1 | a0001c0002t0002g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2000+2622A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79802970 | ||||||
| chr12:79803198
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2000+2394G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79803198 | ||||||
| chr12:79803269
|
G | A | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2000+2323C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79803269 | ||||||
| chr12:79803457
|
A | G | 1 | a0001c0002t0002g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2000+2135T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79803457 | ||||||
| chr12:79803547
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2000+2045T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79803547 | ||||||
| chr12:79803602
|
C | T | 2 | a0001c0001t0003g0180a0001c0001t0003g0181 | 2 | NA18939.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2000+1990G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79803602 | ||||||
| chr12:79803860
|
A | G | 1 | a0001c0001t0004g0285 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2000+1732T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79803860 | ||||||
| chr12:79804631
|
GGTCA | G | 12 | a0001c0001t0001g0130a0001c0001t0004g0298a0001c0001t0004g0299others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.2000+957_2000+960d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79804631 | ||||||
| chr12:79804645
|
T | TA | 11 | a0001c0002t0005g0099a0001c0002t0008g0087a0001c0002t0008g0088others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2000+946dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79804645 | ||||||
| chr12:79804948
|
A | G | 47 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.2000+644T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79804948 | ||||||
| chr12:79805022
|
A | C | 2 | a0001c0002t0008g0087a0001c0002t0008g0088 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2000+570T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79805022 | ||||||
| chr12:79805166
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2000+426G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79805166 | ||||||
| chr12:79805179
|
G | T | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2000+413C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79805179 | ||||||
| chr12:79805407
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2000+185G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79805407 | ||||||
| chr12:79805408
|
G | A | 1 | a0001c0001t0007g0140 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2000+184C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 14/24 | chr12 | 79805408 | ||||||
| chr12:79805881
|
G | T | 3 | a0001c0002t0002g0044a0001c0002t0002g0058a0001c0002t0002g0060 | 3 | HG02083.hp2 HG02132.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1824-113C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 13/24 | chr12 | 79805881 | ||||||
| chr12:79805909
|
C | T | 1 | a0001c0002t0002g0031 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1824-141G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 13/24 | chr12 | 79805909 | ||||||
| chr12:79805980
|
T | C | 2 | a0001c0001t0003g0171a0001c0001t0003g0172 | 2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1823+186A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 13/24 | chr12 | 79805980 | ||||||
| chr12:79806339
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp1 | splice_region_variant&intron_variant | LOW | c.1656-6G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/24 | chr12 | 79806339 | ||||||
| chr12:79806617
|
C | G | 3 | a0001c0001t0001g0206a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG00741.hp1 HG01261.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1656-284G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/24 | chr12 | 79806617 | ||||||
| chr12:79806710
|
A | G | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656-377T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/24 | chr12 | 79806710 | ||||||
| chr12:79806944
|
G | C | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1655+282C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/24 | chr12 | 79806944 | ||||||
| chr12:79807074
|
C | A | 70 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1655+152G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/24 | chr12 | 79807074 | ||||||
| chr12:79807111
|
T | C | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1655+115A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/24 | chr12 | 79807111 | ||||||
| chr12:79807133
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1655+93C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/24 | chr12 | 79807133 | ||||||
| chr12:79807204
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1655+22G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 12/24 | chr12 | 79807204 | ||||||
| chr12:79807491
|
TTA | T | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1551-163_1551-162d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807491 | ||||||
| chr12:79807543
|
A | G | 1 | a0001c0002t0006g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1551-213T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807543 | ||||||
| chr12:79807585
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1551-255C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807585 | ||||||
| chr12:79807664
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1551-334T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807664 | ||||||
| chr12:79807709
|
A | T | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1551-379T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807709 | ||||||
| chr12:79807743
|
T | C | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1551-413A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807743 | ||||||
| chr12:79807761
|
C | T | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1551-431G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807761 | ||||||
| chr12:79807808
|
A | G | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1551-478T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807808 | ||||||
| chr12:79807893
|
T | C | 1 | a0001c0002t0002g0020 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1551-563A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807893 | ||||||
| chr12:79807992
|
C | T | 1 | a0001c0002t0006g0080 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1550+491G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79807992 | ||||||
| chr12:79808021
|
G | A | 1 | a0001c0002t0005g0123 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1550+462C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 11/24 | chr12 | 79808021 | ||||||
| chr12:79809056
|
G | C | 1 | a0004c0004t0005g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1456-479C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809056 | ||||||
| chr12:79809116
|
A | G | 1 | a0001c0002t0009g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1456-539T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809116 | ||||||
| chr12:79809185
|
T | G | 3 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0176 | 3 | NA18944.hp2 NA18969.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1456-608A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809185 | ||||||
| chr12:79809214
|
T | G | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1455+581A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809214 | ||||||
| chr12:79809301
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1455+494G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809301 | ||||||
| chr12:79809339
|
T | C | 1 | a0001c0001t0004g0300 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1455+456A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809339 | ||||||
| chr12:79809405
|
T | C | 3 | a0001c0002t0002g0044a0001c0002t0002g0058a0001c0002t0002g0060 | 3 | HG02083.hp2 HG02132.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1455+390A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809405 | ||||||
| chr12:79809560
|
G | A | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1455+235C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809560 | ||||||
| chr12:79809737
|
G | A | 1 | a0001c0002t0008g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1455+58C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 10/24 | chr12 | 79809737 | ||||||
| chr12:79810051
|
G | T | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1240-41C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810051 | ||||||
| chr12:79810084
|
A | C | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1240-74T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810084 | ||||||
| chr12:79810171
|
T | C | 2 | a0001c0002t0008g0087a0001c0002t0008g0088 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1240-161A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810171 | ||||||
| chr12:79810245
|
T | C | 1 | a0001c0002t0005g0121 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1240-235A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810245 | ||||||
| chr12:79810298
|
C | A | 1 | a0001c0002t0002g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1240-288G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810298 | ||||||
| chr12:79810624
|
T | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1240-614A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810624 | ||||||
| chr12:79810731
|
TA | T | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1240-722delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810731 | ||||||
| chr12:79810884
|
C | CT | 7 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157others(4): Show | 7 | HG01192.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-875dupA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810884 | ||||||
| chr12:79810884
|
CT | C | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1240-875delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810884 | ||||||
| chr12:79810973
|
C | T | 68 | a0001c0001t0003g0006a0001c0001t0003g0128a0001c0001t0003g0129others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1240-963G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79810973 | ||||||
| chr12:79811065
|
A | T | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1240-1055T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811065 | ||||||
| chr12:79811169
|
A | C | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1240-1159T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811169 | ||||||
| chr12:79811237
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240-1227A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811237 | ||||||
| chr12:79811379
|
G | A | 1 | a0001c0002t0008g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240-1369C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811379 | ||||||
| chr12:79811396
|
T | G | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1240-1386A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811396 | ||||||
| chr12:79811674
|
A | T | 4 | a0001c0002t0005g0119a0001c0002t0005g0120a0001c0002t0005g0121others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-1664T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811674 | ||||||
| chr12:79811690
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1240-1680A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811690 | ||||||
| chr12:79811693
|
T | C | 2 | a0001c0001t0003g0132a0001c0001t0003g0149 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1240-1683A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811693 | ||||||
| chr12:79811741
|
T | A | 1 | a0001c0001t0004g0307 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1240-1731A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811741 | ||||||
| chr12:79811890
|
G | T | 3 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009 | 3 | HG02055.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1240-1880C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811890 | ||||||
| chr12:79811956
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | NA18951.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1240-1946C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79811956 | ||||||
| chr12:79812382
|
C | CTGTGTGC others(1): Show |
23 | a0001c0001t0001g0188a0001c0001t0001g0195a0001c0001t0001g0196others(20): Show | 23 | HG00423.hp2 HG00741.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.1240-2373_1240-237 others(12): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812382 | ||||||
| chr12:79812382
|
C | CTGTGTGC others(3): Show |
13 | a0001c0001t0001g0198a0001c0001t0001g0210a0001c0001t0001g0211others(10): Show | 13 | HG00140.hp1 HG00323.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-2373_1240-237 others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812382 | ||||||
| chr12:79812382
|
C | CTGTGTGC others(5): Show |
25 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0199others(22): Show | 25 | HG00323.hp1 HG01074.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1240-2373_1240-237 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812382 | ||||||
| chr12:79812382
|
C | CTGTGTGC others(7): Show |
2 | a0001c0001t0001g0234a0001c0001t0001g0250 | 2 | HG00438.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1240-2373_1240-237 others(18): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812382 | ||||||
| chr12:79812382
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0003g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1240-2373_1240-237 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812382 | ||||||
| chr12:79812382
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0003g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1240-2373_1240-237 others(18): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812382 | ||||||
| chr12:79812383
|
T | TGTGTGC | 3 | a0001c0001t0001g0204a0001c0001t0001g0218a0001c0001t0001g0226 | 3 | HG00639.hp2 HG01975.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1240-2374_1240-237 others(10): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812383 | ||||||
| chr12:79812385
|
T | TGTGC | 5 | a0001c0001t0001g0127a0001c0001t0001g0242a0001c0001t0001g0243others(2): Show | 5 | HG00597.hp2 HG02723.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240-2376_1240-237 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812385 | ||||||
| chr12:79812391
|
C | CGT | 69 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0177others(66): Show | 69 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1240-2383_1240-238 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGT | 10 | a0001c0001t0003g0157a0001c0001t0003g0166a0001c0002t0002g0044others(7): Show | 10 | HG01192.hp1 HG02280.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1240-2385_1240-238 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGT | 7 | a0001c0001t0003g0159a0001c0001t0004g0273a0001c0002t0002g0042others(4): Show | 7 | HG00741.hp2 HG01099.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-2387_1240-238 others(10): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(1): Show |
31 | a0001c0001t0001g0241a0001c0001t0003g0148a0001c0001t0003g0170others(28): Show | 32 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1240-2389_1240-238 others(12): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(3): Show |
17 | a0001c0001t0003g0128a0001c0001t0003g0169a0001c0001t0003g0182others(14): Show | 17 | HG01109.hp2 HG01975.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.1240-2391_1240-238 others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(5): Show |
50 | a0001c0001t0001g0130a0001c0001t0003g0006a0001c0001t0003g0144others(47): Show | 50 | HG00544.hp1 HG00639.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1240-2393_1240-238 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(7): Show |
21 | a0001c0001t0003g0133a0001c0001t0003g0146a0001c0001t0003g0158others(18): Show | 21 | HG00408.hp2 HG01074.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1240-2395_1240-238 others(18): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(9): Show |
6 | a0001c0001t0004g0301a0001c0001t0004g0307a0001c0001t0007g0137others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-2397_1240-238 others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(11): Show |
4 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-2399_1240-238 others(22): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(13): Show |
6 | a0001c0001t0004g0275a0001c0001t0004g0284a0001c0001t0007g0139others(3): Show | 6 | HG02040.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-2401_1240-238 others(24): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(15): Show |
1 | a0001c0001t0007g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1240-2403_1240-238 others(26): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | CGTGTGTG others(19): Show |
1 | a0001c0001t0007g0140 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1240-2407_1240-238 others(30): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
C | T | 74 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(71): Show | 74 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1240-2381G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812391
|
CGT | C | 4 | a0001c0002t0002g0062a0001c0002t0008g0095a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-2383_1240-238 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812391 | ||||||
| chr12:79812658
|
GTCTATTC others(25): Show |
G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240-2680_1240-264 others(36): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812658 | ||||||
| chr12:79812801
|
G | A | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1240-2791C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79812801 | ||||||
| chr12:79813070
|
C | T | 46 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(43): Show | 47 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1240-3060G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79813070 | ||||||
| chr12:79813103
|
T | A | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1240-3093A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79813103 | ||||||
| chr12:79813214
|
A | G | 1 | a0001c0002t0006g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1240-3204T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79813214 | ||||||
| chr12:79813290
|
G | T | 124 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(121): Show | 124 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1240-3280C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79813290 | ||||||
| chr12:79813295
|
C | T | 1 | a0001c0001t0004g0305 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1240-3285G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79813295 | ||||||
| chr12:79813732
|
T | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0128a0001c0001t0003g0129others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1239+3662A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79813732 | ||||||
| chr12:79814037
|
C | G | 1 | a0001c0002t0002g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1239+3357G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814037 | ||||||
| chr12:79814103
|
A | G | 51 | a0001c0001t0003g0006a0001c0001t0003g0129a0001c0001t0003g0133others(48): Show | 51 | HG00408.hp2 HG00544.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1239+3291T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814103 | ||||||
| chr12:79814178
|
TAAG | T | 3 | a0001c0001t0003g0162a0001c0001t0003g0168a0001c0001t0003g0169 | 3 | HG02074.hp2 NA18993.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1239+3213_1239+321 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814178 | ||||||
| chr12:79814241
|
G | A | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+3153C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814241 | ||||||
| chr12:79814248
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1239+3146G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814248 | ||||||
| chr12:79814259
|
C | T | 56 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1239+3135G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814259 | ||||||
| chr12:79814441
|
C | T | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1239+2953G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814441 | ||||||
| chr12:79814476
|
C | CA | 68 | a0001c0001t0001g0221a0001c0001t0001g0239a0001c0001t0001g0240others(65): Show | 68 | HG00408.hp1 HG00544.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.1239+2917dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814476 | ||||||
| chr12:79814476
|
C | CAA | 11 | a0001c0001t0004g0295a0001c0001t0004g0298a0001c0001t0004g0299others(8): Show | 11 | HG01928.hp1 HG02015.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1239+2916_1239+291 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814476 | ||||||
| chr12:79814498
|
AAAG | A | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+2893_1239+289 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814498 | ||||||
| chr12:79814500
|
AG | A | 19 | a0001c0001t0001g0197a0001c0001t0003g0132a0001c0001t0003g0144others(16): Show | 19 | HG00639.hp1 HG01109.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.1239+2893delC | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814500 | ||||||
| chr12:79814501
|
G | A | 283 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(280): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1239+2893C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814501 | ||||||
| chr12:79814764
|
G | A | 1 | a0001c0001t0007g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1239+2630C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814764 | ||||||
| chr12:79814815
|
C | CA | 131 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(128): Show | 132 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1239+2578dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814815 | ||||||
| chr12:79814815
|
C | CAA | 74 | a0001c0001t0001g0201a0001c0001t0001g0222a0001c0001t0001g0224others(71): Show | 74 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1239+2577_1239+257 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814815 | ||||||
| chr12:79814815
|
C | CAAA | 14 | a0001c0001t0003g0132a0001c0001t0003g0151a0001c0001t0003g0152others(11): Show | 14 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1239+2576_1239+257 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814815 | ||||||
| chr12:79814815
|
CA | C | 10 | a0001c0002t0002g0041a0001c0002t0002g0061a0001c0002t0002g0074others(7): Show | 10 | HG01243.hp1 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1239+2578delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814815 | ||||||
| chr12:79814842
|
T | A | 1 | a0001c0002t0005g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1239+2552A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79814842 | ||||||
| chr12:79815034
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1239+2360T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815034 | ||||||
| chr12:79815073
|
C | A | 181 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(178): Show | 182 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1239+2321G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815073 | ||||||
| chr12:79815144
|
T | C | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1239+2250A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815144 | ||||||
| chr12:79815275
|
C | T | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1239+2119G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815275 | ||||||
| chr12:79815320
|
G | A | 30 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1239+2074C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815320 | ||||||
| chr12:79815367
|
A | G | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1239+2027T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815367 | ||||||
| chr12:79815445
|
C | T | 69 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(66): Show | 69 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1239+1949G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815445 | ||||||
| chr12:79815507
|
C | T | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1239+1887G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815507 | ||||||
| chr12:79815515
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1239+1879G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815515 | ||||||
| chr12:79815524
|
GA | G | 9 | a0001c0001t0001g0212a0001c0001t0001g0235a0001c0002t0009g0010others(6): Show | 9 | HG01074.hp2 HG01496.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+1869delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815524 | ||||||
| chr12:79815571
|
G | A | 1 | a0001c0001t0004g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1239+1823C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815571 | ||||||
| chr12:79815601
|
A | G | 1 | a0001c0002t0002g0023 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1239+1793T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815601 | ||||||
| chr12:79815875
|
A | G | 1 | a0001c0002t0008g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1239+1519T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815875 | ||||||
| chr12:79815888
|
G | A | 2 | a0001c0002t0006g0030a0001c0002t0006g0078 | 2 | NA18988.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1239+1506C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815888 | ||||||
| chr12:79815981
|
AT | A | 168 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(165): Show | 169 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1239+1412delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79815981 | ||||||
| chr12:79816055
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1239+1339A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79816055 | ||||||
| chr12:79816137
|
C | T | 1 | a0001c0002t0002g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1239+1257G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79816137 | ||||||
| chr12:79816190
|
T | G | 7 | a0001c0002t0006g0075a0001c0002t0006g0080a0001c0002t0006g0081others(4): Show | 7 | NA18939.hp1 NA18961.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+1204A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79816190 | ||||||
| chr12:79816217
|
G | A | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1239+1177C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79816217 | ||||||
| chr12:79816378
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1239+1016C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79816378 | ||||||
| chr12:79817051
|
G | A | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+343C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79817051 | ||||||
| chr12:79817075
|
GA | G | 67 | a0001c0001t0003g0006a0001c0001t0003g0128a0001c0001t0003g0129others(64): Show | 67 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1239+318delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79817075 | ||||||
| chr12:79817140
|
T | C | 1 | a0001c0002t0002g0035 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1239+254A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79817140 | ||||||
| chr12:79817202
|
T | G | 1 | a0001c0001t0001g0219 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1239+192A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 9/24 | chr12 | 79817202 | ||||||
| chr12:79817661
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1115-143T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79817661 | ||||||
| chr12:79817756
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1115-238A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79817756 | ||||||
| chr12:79817840
|
C | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-322G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79817840 | ||||||
| chr12:79817854
|
C | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1115-336G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79817854 | ||||||
| chr12:79818035
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1115-517T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818035 | ||||||
| chr12:79818227
|
C | CCCATGTA others(3): Show |
1 | a0001c0001t0003g0164 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1115-719_1115-710d others(12): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818227 | ||||||
| chr12:79818284
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1115-766G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818284 | ||||||
| chr12:79818344
|
C | T | 47 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1115-826G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818344 | ||||||
| chr12:79818415
|
G | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1115-897C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818415 | ||||||
| chr12:79818444
|
T | C | 51 | a0001c0001t0003g0006a0001c0001t0003g0129a0001c0001t0003g0133others(48): Show | 51 | HG00408.hp2 HG00544.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1115-926A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818444 | ||||||
| chr12:79818760
|
A | C | 6 | a0001c0001t0004g0271a0001c0001t0004g0284a0001c0001t0004g0285others(3): Show | 6 | HG01243.hp2 HG01975.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-1242T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818760 | ||||||
| chr12:79818838
|
A | C | 46 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(43): Show | 47 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1115-1320T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818838 | ||||||
| chr12:79818928
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1115-1410A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79818928 | ||||||
| chr12:79819098
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1115-1580G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79819098 | ||||||
| chr12:79819100
|
A | G | 1 | a0001c0002t0002g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1115-1582T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79819100 | ||||||
| chr12:79819194
|
A | C | 1 | a0001c0001t0004g0287 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1114+1580T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79819194 | ||||||
| chr12:79819547
|
G | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114+1227C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79819547 | ||||||
| chr12:79819918
|
A | G | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1114+856T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79819918 | ||||||
| chr12:79819931
|
T | TA | 16 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0100others(13): Show | 16 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.1114+842dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79819931 | ||||||
| chr12:79819958
|
T | C | 120 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1114+816A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79819958 | ||||||
| chr12:79820046
|
AAAC | A | 121 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(118): Show | 122 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1114+725_1114+727d others(5): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820046 | ||||||
| chr12:79820174
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1114+600A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820174 | ||||||
| chr12:79820293
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1114+481C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820293 | ||||||
| chr12:79820321
|
T | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0216 | 2 | NA18747.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1114+453A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820321 | ||||||
| chr12:79820460
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1114+314T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820460 | ||||||
| chr12:79820538
|
C | CTTTAA | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+231_1114+235d others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820538 | ||||||
| chr12:79820600
|
T | G | 1 | a0001c0001t0007g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1114+174A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820600 | ||||||
| chr12:79820664
|
A | G | 9 | a0001c0002t0002g0015a0001c0002t0002g0017a0001c0002t0002g0018others(6): Show | 9 | HG00438.hp1 HG02040.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114+110T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820664 | ||||||
| chr12:79820678
|
CA | C | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+95delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 8/24 | chr12 | 79820678 | ||||||
| chr12:79820966
|
A | C | 3 | a0001c0002t0002g0069a0001c0002t0002g0070a0001c0002t0002g0071 | 3 | HG02074.hp1 NA18964.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.957-35T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 7/24 | chr12 | 79820966 | ||||||
| chr12:79821320
|
G | A | 70 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.868-154C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 6/24 | chr12 | 79821320 | ||||||
| chr12:79821415
|
G | C | 2 | a0001c0002t0002g0042a0001c0002t0002g0048 | 2 | HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.868-249C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 6/24 | chr12 | 79821415 | ||||||
| chr12:79821509
|
T | C | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.868-343A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 6/24 | chr12 | 79821509 | ||||||
| chr12:79821621
|
C | T | 15 | a0001c0002t0006g0014a0001c0002t0006g0029a0001c0002t0006g0030others(12): Show | 15 | HG03710.hp2 HG03831.hp1 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.868-455G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 6/24 | chr12 | 79821621 | ||||||
| chr12:79821700
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.867+416A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 6/24 | chr12 | 79821700 | ||||||
| chr12:79821728
|
G | A | 1 | a0001c0002t0002g0057 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.867+388C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 6/24 | chr12 | 79821728 | ||||||
| chr12:79821751
|
C | CA | 8 | a0001c0001t0001g0202a0001c0001t0001g0216a0001c0001t0001g0226others(5): Show | 8 | HG00639.hp2 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.867+364dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 6/24 | chr12 | 79821751 | ||||||
| chr12:79821836
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.867+280G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 6/24 | chr12 | 79821836 | ||||||
| chr12:79822280
|
C | A | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.793-90G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79822280 | ||||||
| chr12:79822433
|
T | C | 2 | a0001c0001t0003g0144a0001c0001t0003g0147 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.793-243A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79822433 | ||||||
| chr12:79822440
|
C | A | 1 | a0001c0002t0005g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.793-250G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79822440 | ||||||
| chr12:79822493
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.793-303C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79822493 | ||||||
| chr12:79822495
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.793-305T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79822495 | ||||||
| chr12:79822561
|
T | G | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-371A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79822561 | ||||||
| chr12:79822811
|
AT | A | 158 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(155): Show | 159 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.793-622delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79822811 | ||||||
| chr12:79823194
|
G | C | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.793-1004C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823194 | ||||||
| chr12:79823222
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793-1032A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823222 | ||||||
| chr12:79823233
|
T | A | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.793-1043A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823233 | ||||||
| chr12:79823244
|
C | T | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.793-1054G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823244 | ||||||
| chr12:79823262
|
A | T | 1 | a0001c0002t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.793-1072T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823262 | ||||||
| chr12:79823419
|
G | A | 1 | a0001c0002t0002g0004 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.793-1229C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823419 | ||||||
| chr12:79823592
|
CT | C | 240 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(237): Show | 241 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.793-1403delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823592 | ||||||
| chr12:79823592
|
CTT | C | 9 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0003g0157others(6): Show | 9 | HG01074.hp2 HG01943.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.793-1404_793-1403d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823592 | ||||||
| chr12:79823597
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793-1407A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823597 | ||||||
| chr12:79823661
|
G | A | 1 | a0001c0002t0006g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.793-1471C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823661 | ||||||
| chr12:79823898
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.793-1708T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79823898 | ||||||
| chr12:79824186
|
A | G | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-1996T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79824186 | ||||||
| chr12:79824290
|
G | A | 2 | a0001c0001t0003g0132a0001c0001t0003g0149 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.793-2100C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79824290 | ||||||
| chr12:79824319
|
C | G | 2 | a0001c0001t0004g0268a0001c0001t0004g0269 | 2 | HG00408.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.793-2129G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79824319 | ||||||
| chr12:79824357
|
C | A | 1 | a0001c0002t0006g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.793-2167G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79824357 | ||||||
| chr12:79824488
|
C | T | 1 | a0001c0001t0004g0275 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.793-2298G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79824488 | ||||||
| chr12:79824541
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.793-2351G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79824541 | ||||||
| chr12:79824579
|
A | G | 1 | a0001c0001t0004g0293 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.793-2389T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79824579 | ||||||
| chr12:79824696
|
T | G | 5 | a0001c0002t0002g0035a0001c0002t0002g0052a0001c0002t0002g0053others(2): Show | 5 | NA18943.hp1 NA18948.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-2506A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79824696 | ||||||
| chr12:79825035
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0216 | 2 | NA18747.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.793-2845T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79825035 | ||||||
| chr12:79825204
|
G | T | 1 | a0001c0001t0003g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.793-3014C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79825204 | ||||||
| chr12:79825270
|
G | C | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.792+3050C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79825270 | ||||||
| chr12:79825272
|
C | T | 1 | a0001c0002t0008g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.792+3048G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79825272 | ||||||
| chr12:79825825
|
A | G | 1 | a0001c0002t0005g0124 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.792+2495T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79825825 | ||||||
| chr12:79826108
|
G | T | 240 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0003g0006others(237): Show | 241 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.792+2212C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79826108 | ||||||
| chr12:79826129
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.792+2191G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79826129 | ||||||
| chr12:79826337
|
G | GT | 39 | a0001c0001t0001g0204a0001c0001t0001g0211a0001c0001t0001g0212others(36): Show | 39 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.792+1982dupA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79826337 | ||||||
| chr12:79826337
|
GT | G | 81 | a0001c0001t0003g0149a0001c0001t0004g0293a0001c0002t0002g0004others(78): Show | 81 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.792+1982delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79826337 | ||||||
| chr12:79826487
|
T | C | 120 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.792+1833A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79826487 | ||||||
| chr12:79826544
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.792+1776G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79826544 | ||||||
| chr12:79826580
|
A | G | 2 | a0001c0002t0002g0046a0001c0002t0002g0068 | 2 | HG00423.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.792+1740T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79826580 | ||||||
| chr12:79826976
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0004g0283 | 2 | NA18977.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.792+1344C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79826976 | ||||||
| chr12:79827054
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.792+1266C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79827054 | ||||||
| chr12:79827175
|
A | G | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.792+1145T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79827175 | ||||||
| chr12:79827467
|
A | G | 2 | a0001c0002t0002g0042a0001c0002t0002g0048 | 2 | HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.792+853T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79827467 | ||||||
| chr12:79827723
|
T | C | 46 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(43): Show | 47 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.792+597A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79827723 | ||||||
| chr12:79827823
|
G | T | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+497C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79827823 | ||||||
| chr12:79827828
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.792+492T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79827828 | ||||||
| chr12:79828066
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.792+254A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79828066 | ||||||
| chr12:79828132
|
T | A | 1 | a0001c0001t0004g0301 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.792+188A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79828132 | ||||||
| chr12:79828135
|
G | A | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+185C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 5/24 | chr12 | 79828135 | ||||||
| chr12:79828495
|
T | C | 1 | a0001c0002t0002g0057 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.648-31A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79828495 | ||||||
| chr12:79828664
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.648-200T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79828664 | ||||||
| chr12:79828997
|
T | C | 1 | a0001c0001t0004g0291 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.648-533A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79828997 | ||||||
| chr12:79829067
|
T | C | 1 | a0001c0002t0002g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.648-603A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829067 | ||||||
| chr12:79829067
|
T | TA | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.648-604dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829067 | ||||||
| chr12:79829330
|
C | G | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.648-866G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829330 | ||||||
| chr12:79829493
|
G | C | 254 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(251): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.648-1029C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829493 | ||||||
| chr12:79829503
|
C | T | 1 | a0001c0002t0002g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.648-1039G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829503 | ||||||
| chr12:79829835
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.648-1371C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829835 | ||||||
| chr12:79829882
|
C | G | 1 | a0001c0001t0004g0306 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.648-1418G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829882 | ||||||
| chr12:79829918
|
C | G | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.648-1454G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829918 | ||||||
| chr12:79829936
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.648-1472T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79829936 | ||||||
| chr12:79830102
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648-1638A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830102 | ||||||
| chr12:79830103
|
TA | T | 6 | a0001c0001t0001g0219a0001c0001t0003g0165a0001c0002t0009g0010others(3): Show | 6 | HG01168.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.648-1640delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830103 | ||||||
| chr12:79830147
|
C | G | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.648-1683G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830147 | ||||||
| chr12:79830326
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1862G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830326 | ||||||
| chr12:79830341
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.648-1877A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830341 | ||||||
| chr12:79830420
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.647+1912T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830420 | ||||||
| chr12:79830640
|
C | T | 240 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0003g0006others(237): Show | 241 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.647+1692G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830640 | ||||||
| chr12:79830705
|
C | T | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.647+1627G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830705 | ||||||
| chr12:79830867
|
A | T | 17 | a0001c0001t0003g0128a0001c0001t0003g0132a0001c0001t0003g0144others(14): Show | 17 | HG00639.hp1 HG01109.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.647+1465T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79830867 | ||||||
| chr12:79831151
|
C | CA | 11 | a0001c0001t0003g0144a0001c0001t0003g0147a0001c0001t0003g0148others(8): Show | 11 | HG00639.hp1 HG01109.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.647+1180dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79831151 | ||||||
| chr12:79831168
|
T | C | 1 | a0001c0001t0004g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.647+1164A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79831168 | ||||||
| chr12:79831910
|
G | C | 121 | a0001c0001t0001g0204a0001c0002t0002g0004a0001c0002t0002g0013others(118): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.647+422C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79831910 | ||||||
| chr12:79831955
|
A | G | 14 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0177others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.647+377T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79831955 | ||||||
| chr12:79831966
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.647+366G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79831966 | ||||||
| chr12:79832095
|
A | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.647+237T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79832095 | ||||||
| chr12:79832207
|
A | G | 47 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.647+125T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 4/24 | chr12 | 79832207 | ||||||
| chr12:79832753
|
G | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.488-262C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79832753 | ||||||
| chr12:79832759
|
T | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.488-268A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79832759 | ||||||
| chr12:79832827
|
G | A | 1 | a0001c0002t0002g0069 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.488-336C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79832827 | ||||||
| chr12:79833185
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-694G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833185 | ||||||
| chr12:79833255
|
A | G | 1 | a0001c0001t0007g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.488-764T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833255 | ||||||
| chr12:79833439
|
C | T | 2 | a0001c0002t0008g0096a0001c0002t0008g0098 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.488-948G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833439 | ||||||
| chr12:79833514
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.488-1023T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833514 | ||||||
| chr12:79833520
|
G | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.488-1029C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833520 | ||||||
| chr12:79833648
|
C | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.488-1157G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833648 | ||||||
| chr12:79833670
|
CA | C | 229 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(226): Show | 230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.488-1180delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833670 | ||||||
| chr12:79833726
|
A | G | 2 | a0001c0001t0007g0135a0001c0001t0007g0142 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.488-1235T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833726 | ||||||
| chr12:79833729
|
TG | T | 9 | a0001c0001t0001g0241a0001c0001t0004g0001a0001c0001t0004g0273others(6): Show | 10 | HG00673.hp1 NA18956.hp1 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.488-1239delC | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833729 | ||||||
| chr12:79833768
|
T | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0128a0001c0001t0003g0129others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.488-1277A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833768 | ||||||
| chr12:79833830
|
T | C | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.488-1339A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833830 | ||||||
| chr12:79833846
|
G | GA | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0194others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.488-1356dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833846 | ||||||
| chr12:79833846
|
G | GAA | 14 | a0001c0001t0001g0188a0001c0001t0001g0221a0001c0001t0001g0236others(11): Show | 14 | HG02027.hp2 HG02055.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.488-1357_488-1356d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79833846 | ||||||
| chr12:79834140
|
CAAGGA | C | 4 | a0001c0001t0001g0196a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG01934.hp1 HG01943.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-1654_488-1650d others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79834140 | ||||||
| chr12:79834466
|
T | A | 1 | a0001c0002t0005g0121 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.488-1975A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79834466 | ||||||
| chr12:79834553
|
G | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.488-2062C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79834553 | ||||||
| chr12:79834554
|
T | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.488-2063A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79834554 | ||||||
| chr12:79834617
|
T | C | 2 | a0001c0002t0006g0079a0001c0002t0009g0094 | 2 | HG02258.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.488-2126A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79834617 | ||||||
| chr12:79834663
|
C | T | 5 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0221others(2): Show | 5 | HG00323.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-2172G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79834663 | ||||||
| chr12:79834716
|
GTAGGAGA others(6): Show |
G | 1 | a0001c0001t0001g0244 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.488-2238_488-2226d others(15): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79834716 | ||||||
| chr12:79834717
|
T | C | 1 | a0001c0002t0002g0055 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.488-2226A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79834717 | ||||||
| chr12:79835104
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.488-2613C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835104 | ||||||
| chr12:79835119
|
C | T | 2 | a0001c0002t0008g0096a0001c0002t0008g0098 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.488-2628G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835119 | ||||||
| chr12:79835255
|
C | T | 2 | a0001c0001t0003g0171a0001c0001t0003g0172 | 2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.488-2764G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835255 | ||||||
| chr12:79835265
|
T | C | 1 | a0001c0001t0003g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.488-2774A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835265 | ||||||
| chr12:79835288
|
C | A | 1 | a0001c0001t0003g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488-2797G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835288 | ||||||
| chr12:79835464
|
AC | A | 3 | a0001c0001t0003g0157a0001c0001t0003g0159a0001c0001t0003g0166 | 3 | HG00741.hp2 HG01192.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.488-2974delG | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835464 | ||||||
| chr12:79835534
|
G | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.488-3043C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835534 | ||||||
| chr12:79835546
|
C | T | 1 | a0001c0002t0005g0123 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.488-3055G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835546 | ||||||
| chr12:79835981
|
A | G | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.488-3490T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79835981 | ||||||
| chr12:79836145
|
T | C | 3 | a0001c0002t0002g0038a0001c0002t0002g0039a0001c0002t0002g0040 | 3 | HG04199.hp2 NA19000.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.488-3654A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79836145 | ||||||
| chr12:79836174
|
A | T | 1 | a0001c0001t0014g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.488-3683T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79836174 | ||||||
| chr12:79836175
|
T | A | 1 | a0001c0001t0014g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.488-3684A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79836175 | ||||||
| chr12:79836176
|
A | T | 1 | a0001c0001t0014g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.488-3685T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79836176 | ||||||
| chr12:79836395
|
G | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.488-3904C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79836395 | ||||||
| chr12:79836543
|
CT | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-4053delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79836543 | ||||||
| chr12:79836794
|
A | T | 1 | a0001c0001t0004g0311 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.488-4303T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79836794 | ||||||
| chr12:79836913
|
T | C | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.488-4422A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79836913 | ||||||
| chr12:79837285
|
G | T | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.488-4794C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79837285 | ||||||
| chr12:79837341
|
T | C | 1 | a0001c0002t0005g0125 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.488-4850A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79837341 | ||||||
| chr12:79837345
|
T | C | 1 | a0001c0001t0003g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.488-4854A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79837345 | ||||||
| chr12:79837627
|
G | C | 1 | a0001c0001t0004g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.488-5136C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79837627 | ||||||
| chr12:79837893
|
G | A | 2 | a0001c0001t0003g0150a0001c0001t0003g0152 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-5402C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79837893 | ||||||
| chr12:79838153
|
A | C | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-5662T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79838153 | ||||||
| chr12:79838172
|
G | T | 1 | a0001c0001t0004g0307 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488-5681C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79838172 | ||||||
| chr12:79838293
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.488-5802A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79838293 | ||||||
| chr12:79838429
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.488-5938C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79838429 | ||||||
| chr12:79838434
|
G | A | 2 | a0001c0002t0006g0076a0001c0002t0006g0077 | 2 | NA18981.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.488-5943C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79838434 | ||||||
| chr12:79838448
|
T | C | 1 | a0001c0001t0018g0266 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.488-5957A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79838448 | ||||||
| chr12:79838673
|
T | C | 1 | a0006c0007t0009g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.488-6182A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79838673 | ||||||
| chr12:79838913
|
C | T | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.487+6389G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79838913 | ||||||
| chr12:79839125
|
A | G | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+6177T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79839125 | ||||||
| chr12:79839176
|
C | T | 251 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(248): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.487+6126G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79839176 | ||||||
| chr12:79839727
|
T | C | 1 | a0001c0002t0002g0068 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.487+5575A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79839727 | ||||||
| chr12:79839785
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.487+5517A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79839785 | ||||||
| chr12:79839886
|
G | C | 1 | a0001c0001t0001g0203 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.487+5416C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79839886 | ||||||
| chr12:79840052
|
AT | A | 47 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.487+5249delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840052 | ||||||
| chr12:79840156
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.487+5146A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840156 | ||||||
| chr12:79840200
|
T | TG | 10 | a0001c0001t0001g0229a0001c0001t0001g0240a0001c0001t0001g0257others(7): Show | 10 | HG00741.hp1 HG02027.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.487+5101dupC | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840200 | ||||||
| chr12:79840397
|
C | G | 2 | a0001c0001t0004g0268a0001c0001t0004g0269 | 2 | HG00408.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.487+4905G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840397 | ||||||
| chr12:79840419
|
T | A | 47 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.487+4883A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840419 | ||||||
| chr12:79840466
|
C | G | 1 | a0001c0001t0003g0180 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.487+4836G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840466 | ||||||
| chr12:79840696
|
C | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487+4606G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840696 | ||||||
| chr12:79840770
|
C | T | 1 | a0001c0002t0008g0087 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487+4532G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840770 | ||||||
| chr12:79840771
|
G | A | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.487+4531C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840771 | ||||||
| chr12:79840842
|
A | G | 1 | a0001c0001t0003g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.487+4460T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840842 | ||||||
| chr12:79840961
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.487+4341C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840961 | ||||||
| chr12:79840971
|
T | C | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+4331A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79840971 | ||||||
| chr12:79841051
|
T | TA | 10 | a0001c0001t0001g0206a0001c0001t0001g0252a0001c0001t0004g0274others(7): Show | 10 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+4250dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841051 | ||||||
| chr12:79841051
|
TA | T | 12 | a0001c0001t0001g0219a0001c0001t0004g0276a0001c0001t0004g0293others(9): Show | 12 | HG00140.hp2 HG01168.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.487+4250delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841051 | ||||||
| chr12:79841068
|
A | G | 4 | a0001c0001t0001g0201a0001c0001t0001g0247a0001c0002t0010g0007others(1): Show | 4 | HG02055.hp2 HG02145.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+4234T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841068 | ||||||
| chr12:79841092
|
C | T | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+4210G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841092 | ||||||
| chr12:79841231
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487+4071G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841231 | ||||||
| chr12:79841234
|
A | C | 4 | a0001c0002t0005g0101a0001c0002t0005g0102a0001c0002t0005g0103others(1): Show | 4 | HG01261.hp1 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+4068T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841234 | ||||||
| chr12:79841262
|
C | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.487+4040G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841262 | ||||||
| chr12:79841277
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.487+4025G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841277 | ||||||
| chr12:79841566
|
G | A | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+3736C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841566 | ||||||
| chr12:79841570
|
G | C | 1 | a0001c0002t0005g0111 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.487+3732C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841570 | ||||||
| chr12:79841680
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487+3622T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79841680 | ||||||
| chr12:79842011
|
G | GTT | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.487+3289_487+3290d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842011 | ||||||
| chr12:79842035
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.487+3267C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842035 | ||||||
| chr12:79842047
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.487+3255G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842047 | ||||||
| chr12:79842095
|
G | A | 17 | a0001c0001t0003g0128a0001c0001t0003g0132a0001c0001t0003g0144others(14): Show | 17 | HG00639.hp1 HG01109.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.487+3207C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842095 | ||||||
| chr12:79842181
|
G | A | 1 | a0001c0002t0005g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.487+3121C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842181 | ||||||
| chr12:79842447
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487+2855G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842447 | ||||||
| chr12:79842575
|
T | TGTGTG | 3 | a0001c0001t0003g0129a0001c0001t0004g0297a0001c0003t0015g0086 | 3 | HG02145.hp2 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.487+2726_487+2727i others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
T | TTG | 48 | a0001c0001t0001g0206a0001c0001t0001g0219a0001c0001t0001g0221others(45): Show | 49 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.487+2725_487+2726d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
T | TTGTG | 51 | a0001c0001t0001g0209a0001c0001t0001g0258a0001c0001t0001g0261others(48): Show | 51 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.487+2723_487+2726d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
T | TTGTGTG | 7 | a0001c0001t0003g0186a0001c0001t0003g0192a0001c0001t0004g0288others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+2721_487+2726d others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0003g0166a0001c0001t0007g0135a0001c0002t0010g0265 | 3 | HG01192.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.487+2715_487+2726d others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
TTG | T | 57 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0238others(54): Show | 57 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.487+2725_487+2726d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
TTGTG | T | 8 | a0001c0001t0001g0198a0001c0002t0002g0062a0001c0002t0008g0090others(5): Show | 8 | HG00323.hp2 HG01074.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+2723_487+2726d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
TTGTGTG | T | 6 | a0001c0002t0005g0099a0001c0002t0005g0104a0001c0002t0005g0119others(3): Show | 6 | HG02257.hp1 HG02818.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+2721_487+2726d others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
TTGTGTGT others(1): Show |
T | 50 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0100others(47): Show | 50 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.487+2719_487+2726d others(10): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842575
|
TTGTGTGT others(13): Show |
T | 1 | a0001c0002t0006g0014 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.487+2707_487+2726d others(22): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842575 | ||||||
| chr12:79842585
|
G | A | 4 | a0001c0002t0002g0052a0001c0002t0002g0053a0001c0002t0002g0064others(1): Show | 4 | NA18943.hp1 NA18948.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+2717C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842585 | ||||||
| chr12:79842807
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487+2495C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842807 | ||||||
| chr12:79842891
|
T | C | 47 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.487+2411A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79842891 | ||||||
| chr12:79843030
|
T | C | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.487+2272A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843030 | ||||||
| chr12:79843034
|
G | A | 47 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0004g0001others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.487+2268C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843034 | ||||||
| chr12:79843043
|
GTTTTTGG others(3): Show |
G | 1 | a0001c0001t0001g0219 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.487+2249_487+2258d others(12): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843043 | ||||||
| chr12:79843085
|
A | G | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.487+2217T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843085 | ||||||
| chr12:79843105
|
G | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.487+2197C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843105 | ||||||
| chr12:79843352
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.487+1950C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843352 | ||||||
| chr12:79843378
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.487+1924G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843378 | ||||||
| chr12:79843396
|
T | C | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.487+1906A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843396 | ||||||
| chr12:79843503
|
C | T | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.487+1799G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843503 | ||||||
| chr12:79843611
|
A | AATATAG | 16 | a0001c0001t0001g0127a0001c0001t0001g0194a0001c0001t0001g0204others(13): Show | 16 | HG02258.hp1 HG02559.hp1 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+1685_487+1690d others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843611
|
A | AATATAGA others(5): Show |
1 | a0001c0001t0003g0169 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.487+1679_487+1690d others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843611
|
A | AATATAGA others(11): Show |
1 | a0001c0001t0001g0216 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.487+1673_487+1690d others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843611
|
AATATAG | A | 78 | a0001c0001t0001g0188a0001c0001t0001g0197a0001c0001t0001g0201others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.487+1685_487+1690d others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843611
|
AATATAGA others(5): Show |
A | 48 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0199others(45): Show | 49 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.487+1679_487+1690d others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843611
|
AATATAGA others(11): Show |
A | 22 | a0001c0001t0003g0133a0001c0001t0004g0271a0001c0001t0004g0286others(19): Show | 22 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.487+1673_487+1690d others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843611
|
AATATAGA others(17): Show |
A | 70 | a0001c0001t0001g0221a0001c0002t0002g0004a0001c0002t0002g0013others(67): Show | 70 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.487+1667_487+1690d others(26): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843611
|
AATATAGA others(23): Show |
A | 1 | a0001c0002t0002g0020 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.487+1661_487+1690d others(32): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843611
|
AATATAGA others(29): Show |
A | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1655_487+1690d others(38): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843611 | ||||||
| chr12:79843615
|
T | C | 1 | a0001c0001t0003g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.487+1687A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843615 | ||||||
| chr12:79843653
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.487+1649C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843653 | ||||||
| chr12:79843743
|
C | G | 240 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0003g0006others(237): Show | 241 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.487+1559G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843743 | ||||||
| chr12:79843945
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487+1357A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843945 | ||||||
| chr12:79843998
|
C | G | 1 | a0001c0002t0008g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487+1304G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79843998 | ||||||
| chr12:79844008
|
C | T | 4 | a0001c0002t0005g0105a0001c0002t0005g0107a0001c0002t0005g0108others(1): Show | 4 | HG02809.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1294G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844008 | ||||||
| chr12:79844084
|
T | TTTAA | 3 | a0001c0001t0003g0148a0001c0001t0003g0191a0001c0001t0003g0192 | 3 | HG00639.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.487+1214_487+1217d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844084 | ||||||
| chr12:79844105
|
G | T | 1 | a0001c0001t0003g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.487+1197C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844105 | ||||||
| chr12:79844106
|
T | G | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.487+1196A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844106 | ||||||
| chr12:79844173
|
CTT | C | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.487+1127_487+1128d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844173 | ||||||
| chr12:79844196
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.487+1106G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844196 | ||||||
| chr12:79844199
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487+1103A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844199 | ||||||
| chr12:79844351
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487+951A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844351 | ||||||
| chr12:79844629
|
A | G | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.487+673T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79844629 | ||||||
| chr12:79845035
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487+267T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79845035 | ||||||
| chr12:79845080
|
T | C | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+222A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 3/24 | chr12 | 79845080 | ||||||
| chr12:79845506
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369-86A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845506 | ||||||
| chr12:79845511
|
A | T | 2 | a0001c0002t0005g0106a0001c0002t0005g0111 | 2 | HG01192.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.369-91T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845511 | ||||||
| chr12:79845512
|
G | C | 1 | a0002c0009t0005g0118 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.369-92C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845512 | ||||||
| chr12:79845570
|
G | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-150C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845570 | ||||||
| chr12:79845625
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.369-205G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845625 | ||||||
| chr12:79845697
|
G | A | 1 | a0001c0002t0002g0019 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.369-277C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845697 | ||||||
| chr12:79845709
|
G | A | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.369-289C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845709 | ||||||
| chr12:79845891
|
C | CAAAAATT others(33): Show |
196 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(193): Show | 197 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.369-472_369-471ins others(40): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845891 | ||||||
| chr12:79845991
|
C | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0128a0001c0001t0003g0129others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.369-571G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79845991 | ||||||
| chr12:79846074
|
A | G | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-654T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846074 | ||||||
| chr12:79846104
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-684A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846104 | ||||||
| chr12:79846145
|
T | TTTTA | 240 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0003g0006others(237): Show | 241 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.369-729_369-726dup others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846145 | ||||||
| chr12:79846211
|
T | G | 1 | a0001c0006t0002g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.369-791A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846211 | ||||||
| chr12:79846345
|
C | T | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-925G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846345 | ||||||
| chr12:79846425
|
T | G | 1 | a0001c0002t0006g0014 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.369-1005A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846425 | ||||||
| chr12:79846437
|
C | CTT | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.369-1018_369-1017i others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846437 | ||||||
| chr12:79846487
|
C | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.369-1067G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846487 | ||||||
| chr12:79846539
|
C | G | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369-1119G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846539 | ||||||
| chr12:79846594
|
TCA | T | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-1176_369-1175d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846594 | ||||||
| chr12:79846596
|
A | AT | 18 | a0001c0001t0001g0240a0001c0001t0001g0257a0001c0001t0003g0157others(15): Show | 18 | HG01192.hp1 HG01192.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.369-1177dupA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846596 | ||||||
| chr12:79846681
|
G | A | 1 | a0001c0001t0004g0278 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.369-1261C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846681 | ||||||
| chr12:79846810
|
A | C | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.369-1390T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846810 | ||||||
| chr12:79846937
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.369-1517G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846937 | ||||||
| chr12:79846960
|
C | T | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.369-1540G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79846960 | ||||||
| chr12:79847048
|
C | T | 124 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(121): Show | 124 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.369-1628G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847048 | ||||||
| chr12:79847085
|
C | A | 34 | a0001c0001t0001g0241a0001c0001t0004g0001a0001c0001t0004g0268others(31): Show | 35 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.369-1665G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847085 | ||||||
| chr12:79847365
|
C | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.369-1945G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847365 | ||||||
| chr12:79847374
|
T | A | 11 | a0001c0001t0001g0130a0001c0001t0004g0298a0001c0001t0004g0299others(8): Show | 11 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.369-1954A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847374 | ||||||
| chr12:79847493
|
T | A | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.369-2073A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847493 | ||||||
| chr12:79847593
|
T | C | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.369-2173A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847593 | ||||||
| chr12:79847712
|
T | A | 1 | a0001c0002t0005g0123 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.369-2292A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847712 | ||||||
| chr12:79847713
|
G | A | 68 | a0001c0001t0003g0006a0001c0001t0003g0128a0001c0001t0003g0129others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.369-2293C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847713 | ||||||
| chr12:79847922
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-2502T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847922 | ||||||
| chr12:79847986
|
G | A | 1 | a0001c0002t0008g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.369-2566C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79847986 | ||||||
| chr12:79848084
|
G | A | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.369-2664C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848084 | ||||||
| chr12:79848396
|
T | C | 1 | a0001c0001t0019g0272 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.369-2976A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848396 | ||||||
| chr12:79848477
|
A | G | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.369-3057T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848477 | ||||||
| chr12:79848531
|
T | G | 1 | a0001c0001t0004g0283 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.369-3111A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848531 | ||||||
| chr12:79848636
|
C | T | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.369-3216G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848636 | ||||||
| chr12:79848664
|
C | T | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.369-3244G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848664 | ||||||
| chr12:79848781
|
A | C | 1 | a0001c0001t0003g0189 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.369-3361T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848781 | ||||||
| chr12:79848785
|
C | G | 1 | a0001c0001t0004g0287 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.369-3365G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848785 | ||||||
| chr12:79848901
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-3481C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79848901 | ||||||
| chr12:79849198
|
A | G | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.369-3778T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849198 | ||||||
| chr12:79849335
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-3915G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849335 | ||||||
| chr12:79849395
|
GA | G | 183 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(180): Show | 184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.369-3976delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849395 | ||||||
| chr12:79849397
|
A | G | 1 | a0001c0001t0003g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.369-3977T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849397 | ||||||
| chr12:79849402
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-3982T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849402 | ||||||
| chr12:79849534
|
G | T | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.369-4114C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849534 | ||||||
| chr12:79849550
|
G | C | 120 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.369-4130C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849550 | ||||||
| chr12:79849606
|
A | AAAAC | 3 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296 | 3 | HG02165.hp2 NA18948.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.369-4190_369-4187d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849606 | ||||||
| chr12:79849626
|
C | A | 1 | a0001c0002t0008g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369-4206G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849626 | ||||||
| chr12:79849964
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-4544G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849964 | ||||||
| chr12:79849972
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.369-4552A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79849972 | ||||||
| chr12:79850068
|
T | A | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369-4648A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850068 | ||||||
| chr12:79850081
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.369-4661C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850081 | ||||||
| chr12:79850331
|
G | A | 1 | a0001c0002t0002g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.369-4911C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850331 | ||||||
| chr12:79850496
|
A | T | 4 | a0001c0002t0005g0119a0001c0002t0005g0120a0001c0002t0005g0121others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-5076T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850496 | ||||||
| chr12:79850673
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-5253A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850673 | ||||||
| chr12:79850814
|
G | C | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.369-5394C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850814 | ||||||
| chr12:79850873
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.369-5453G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850873 | ||||||
| chr12:79850917
|
C | T | 17 | a0001c0002t0002g0043a0001c0002t0002g0045a0001c0002t0002g0047others(14): Show | 17 | HG00673.hp2 HG02027.hp1 NA18747.hp2 others(14): Show |
intron_variant | MODIFIER | c.369-5497G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850917 | ||||||
| chr12:79850931
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.369-5511G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79850931 | ||||||
| chr12:79851028
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-5608T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79851028 | ||||||
| chr12:79851053
|
T | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-5633A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79851053 | ||||||
| chr12:79851501
|
C | T | 2 | a0001c0001t0003g0153a0001c0001t0003g0154 | 2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.369-6081G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79851501 | ||||||
| chr12:79851534
|
G | T | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.369-6114C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79851534 | ||||||
| chr12:79851991
|
G | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.369-6571C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79851991 | ||||||
| chr12:79851992
|
C | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.369-6572G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79851992 | ||||||
| chr12:79852193
|
C | CT | 22 | a0001c0001t0003g0128a0001c0001t0003g0132a0001c0001t0003g0144others(19): Show | 22 | HG00639.hp1 HG01109.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.369-6774dupA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79852193 | ||||||
| chr12:79852249
|
G | A | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.369-6829C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79852249 | ||||||
| chr12:79852422
|
C | T | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-7002G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79852422 | ||||||
| chr12:79852489
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.369-7069G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79852489 | ||||||
| chr12:79852627
|
C | T | 2 | a0001c0001t0001g0245a0001c0002t0006g0079 | 2 | HG03831.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.369-7207G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79852627 | ||||||
| chr12:79852771
|
C | A | 30 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.369-7351G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79852771 | ||||||
| chr12:79852797
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.369-7377G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79852797 | ||||||
| chr12:79852809
|
G | A | 1 | a0001c0002t0006g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.369-7389C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79852809 | ||||||
| chr12:79853248
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.369-7828G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79853248 | ||||||
| chr12:79853801
|
G | A | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369-8381C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79853801 | ||||||
| chr12:79853858
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.369-8438A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79853858 | ||||||
| chr12:79853960
|
G | C | 1 | a0001c0001t0003g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.369-8540C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79853960 | ||||||
| chr12:79854149
|
G | A | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.369-8729C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79854149 | ||||||
| chr12:79854843
|
T | G | 30 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.369-9423A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79854843 | ||||||
| chr12:79854980
|
A | AATT | 3 | a0001c0001t0003g0156a0001c0002t0005g0106a0001c0002t0005g0111 | 3 | HG01192.hp2 HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.369-9563_369-9561d others(5): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79854980 | ||||||
| chr12:79855014
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-9594T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855014 | ||||||
| chr12:79855029
|
C | T | 56 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.369-9609G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855029 | ||||||
| chr12:79855082
|
G | A | 2 | a0001c0002t0009g0010a0001c0002t0009g0011 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.369-9662C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855082 | ||||||
| chr12:79855189
|
C | T | 1 | a0001c0001t0012g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369-9769G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855189 | ||||||
| chr12:79855230
|
C | T | 1 | a0001c0001t0004g0275 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.369-9810G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855230 | ||||||
| chr12:79855231
|
G | A | 2 | a0001c0001t0001g0242a0006c0007t0009g0091 | 2 | HG00597.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.369-9811C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855231 | ||||||
| chr12:79855276
|
C | A | 6 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0220others(3): Show | 6 | HG00323.hp2 HG01934.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.369-9856G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855276 | ||||||
| chr12:79855295
|
T | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-9875A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855295 | ||||||
| chr12:79855356
|
T | A | 1 | a0001c0001t0003g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.369-9936A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855356 | ||||||
| chr12:79855430
|
C | T | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369-10010G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855430 | ||||||
| chr12:79855464
|
C | A | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.369-10044G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855464 | ||||||
| chr12:79855477
|
C | T | 51 | a0001c0001t0003g0006a0001c0001t0003g0129a0001c0001t0003g0133others(48): Show | 51 | HG00408.hp2 HG00544.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.369-10057G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855477 | ||||||
| chr12:79855615
|
A | G | 3 | a0001c0002t0006g0030a0001c0002t0006g0078a0001c0002t0006g0079 | 3 | HG03831.hp1 NA18988.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.369-10195T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855615 | ||||||
| chr12:79855741
|
A | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-10321T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855741 | ||||||
| chr12:79855876
|
C | T | 1 | a0005c0005t0003g0185 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.369-10456G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855876 | ||||||
| chr12:79855923
|
A | G | 30 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.369-10503T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79855923 | ||||||
| chr12:79856009
|
C | T | 6 | a0001c0001t0004g0271a0001c0001t0004g0284a0001c0001t0004g0285others(3): Show | 6 | HG01243.hp2 HG01975.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.369-10589G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79856009 | ||||||
| chr12:79856149
|
A | T | 1 | a0001c0001t0003g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.369-10729T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79856149 | ||||||
| chr12:79856285
|
A | T | 120 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.369-10865T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79856285 | ||||||
| chr12:79856369
|
T | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.369-10949A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79856369 | ||||||
| chr12:79856405
|
C | A | 1 | a0001c0001t0004g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.369-10985G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79856405 | ||||||
| chr12:79856787
|
G | GCATTAAC others(5): Show |
1 | a0001c0002t0002g0049 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.369-11379_369-1136 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79856787 | ||||||
| chr12:79857131
|
A | C | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.369-11711T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857131 | ||||||
| chr12:79857132
|
C | T | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.369-11712G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857132 | ||||||
| chr12:79857133
|
G | T | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.369-11713C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857133 | ||||||
| chr12:79857142
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.369-11722A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857142 | ||||||
| chr12:79857212
|
G | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-11792C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857212 | ||||||
| chr12:79857258
|
A | G | 1 | a0001c0001t0003g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.369-11838T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857258 | ||||||
| chr12:79857270
|
A | G | 9 | a0001c0001t0001g0188a0001c0001t0001g0195a0001c0001t0001g0200others(6): Show | 9 | HG00423.hp2 HG02015.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-11850T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857270 | ||||||
| chr12:79857297
|
T | C | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.369-11877A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857297 | ||||||
| chr12:79857374
|
T | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-11954A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857374 | ||||||
| chr12:79857397
|
A | C | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-11977T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857397 | ||||||
| chr12:79857424
|
G | A | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.369-12004C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857424 | ||||||
| chr12:79857550
|
AC | A | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-12131delG | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857550 | ||||||
| chr12:79857568
|
TAATAATA others(6): Show |
T | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-12161_369-1214 others(17): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857568 | ||||||
| chr12:79857827
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | NA18956.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.369-12407A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857827 | ||||||
| chr12:79857850
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369-12430A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857850 | ||||||
| chr12:79857854
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-12434C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857854 | ||||||
| chr12:79857954
|
G | A | 232 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(229): Show | 233 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.369-12534C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857954 | ||||||
| chr12:79857966
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-12546G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79857966 | ||||||
| chr12:79858050
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-12630A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79858050 | ||||||
| chr12:79858105
|
A | T | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.369-12685T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79858105 | ||||||
| chr12:79858457
|
C | T | 1 | a0001c0002t0002g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.369-13037G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79858457 | ||||||
| chr12:79858469
|
T | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.369-13049A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79858469 | ||||||
| chr12:79858485
|
A | G | 310 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(307): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.369-13065T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79858485 | ||||||
| chr12:79858753
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-13333T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79858753 | ||||||
| chr12:79858860
|
G | T | 1 | a0001c0001t0012g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369-13440C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79858860 | ||||||
| chr12:79859002
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-13582G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859002 | ||||||
| chr12:79859114
|
T | C | 2 | a0001c0001t0007g0135a0001c0001t0007g0142 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.368+13694A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859114 | ||||||
| chr12:79859329
|
T | A | 1 | a0001c0002t0005g0125 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.368+13479A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859329 | ||||||
| chr12:79859337
|
T | TA | 6 | a0001c0001t0004g0297a0001c0002t0006g0030a0001c0002t0010g0007others(3): Show | 6 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.368+13470dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859337 | ||||||
| chr12:79859369
|
AC | A | 48 | a0001c0001t0001g0214a0001c0001t0001g0245a0001c0001t0001g0252others(45): Show | 48 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.368+13438delG | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859369 | ||||||
| chr12:79859370
|
C | A | 138 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(135): Show | 139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.368+13438G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859370 | ||||||
| chr12:79859440
|
T | G | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.368+13368A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859440 | ||||||
| chr12:79859681
|
A | G | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+13127T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859681 | ||||||
| chr12:79859726
|
G | A | 1 | a0001c0001t0003g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.368+13082C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859726 | ||||||
| chr12:79859795
|
C | T | 2 | a0001c0001t0003g0162a0001c0001t0003g0168 | 2 | HG02074.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.368+13013G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79859795 | ||||||
| chr12:79860136
|
C | A | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.368+12672G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79860136 | ||||||
| chr12:79860199
|
G | T | 1 | a0001c0002t0005g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.368+12609C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79860199 | ||||||
| chr12:79860219
|
A | G | 1 | a0001c0002t0002g0045 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.368+12589T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79860219 | ||||||
| chr12:79860453
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.368+12355G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79860453 | ||||||
| chr12:79860528
|
C | T | 3 | a0001c0001t0003g0162a0001c0001t0003g0168a0001c0001t0003g0169 | 3 | HG02074.hp2 NA18993.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.368+12280G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79860528 | ||||||
| chr12:79860658
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+12150C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79860658 | ||||||
| chr12:79860858
|
C | CTGG | 3 | a0001c0001t0001g0201a0001c0001t0001g0247a0001c0001t0003g0157 | 3 | HG02735.hp2 NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.368+11947_368+1194 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79860858 | ||||||
| chr12:79860900
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.368+11908G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79860900 | ||||||
| chr12:79861053
|
C | A | 2 | a0001c0002t0002g0025a0001c0002t0002g0028 | 2 | HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.368+11755G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861053 | ||||||
| chr12:79861102
|
T | TTAAACCC | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+11705_368+1170 others(11): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861102 | ||||||
| chr12:79861405
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+11403G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861405 | ||||||
| chr12:79861479
|
G | A | 1 | a0001c0002t0005g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.368+11329C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861479 | ||||||
| chr12:79861482
|
G | C | 1 | a0001c0001t0003g0153 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.368+11326C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861482 | ||||||
| chr12:79861589
|
G | A | 188 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(185): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.368+11219C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861589 | ||||||
| chr12:79861598
|
A | G | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.368+11210T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861598 | ||||||
| chr12:79861659
|
C | T | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.368+11149G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861659 | ||||||
| chr12:79861662
|
C | T | 1 | a0001c0001t0004g0299 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.368+11146G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861662 | ||||||
| chr12:79861664
|
G | A | 1 | a0001c0002t0006g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.368+11144C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861664 | ||||||
| chr12:79861677
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.368+11131G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861677 | ||||||
| chr12:79861687
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+11121C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861687 | ||||||
| chr12:79861740
|
T | C | 1 | a0001c0002t0005g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.368+11068A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861740 | ||||||
| chr12:79861984
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.368+10824G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79861984 | ||||||
| chr12:79862022
|
C | T | 232 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(229): Show | 233 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.368+10786G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862022 | ||||||
| chr12:79862023
|
G | A | 1 | a0001c0002t0006g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.368+10785C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862023 | ||||||
| chr12:79862141
|
T | C | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.368+10667A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862141 | ||||||
| chr12:79862157
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.368+10651A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862157 | ||||||
| chr12:79862270
|
A | G | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.368+10538T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862270 | ||||||
| chr12:79862315
|
A | G | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.368+10493T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862315 | ||||||
| chr12:79862408
|
C | T | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+10400G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862408 | ||||||
| chr12:79862455
|
G | A | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+10353C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862455 | ||||||
| chr12:79862628
|
C | A | 1 | a0001c0001t0003g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.368+10180G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862628 | ||||||
| chr12:79862661
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.368+10147G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862661 | ||||||
| chr12:79862798
|
C | T | 1 | a0001c0001t0004g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.368+10010G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862798 | ||||||
| chr12:79862814
|
T | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+9994A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862814 | ||||||
| chr12:79862822
|
A | C | 3 | a0001c0002t0002g0021a0001c0002t0002g0022a0001c0002t0002g0024 | 3 | HG00438.hp1 NA18977.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.368+9986T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862822 | ||||||
| chr12:79862872
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.368+9936C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862872 | ||||||
| chr12:79862906
|
C | G | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.368+9902G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862906 | ||||||
| chr12:79862986
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.368+9822G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79862986 | ||||||
| chr12:79863454
|
T | C | 1 | a0001c0002t0006g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.368+9354A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863454 | ||||||
| chr12:79863518
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.368+9290G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863518 | ||||||
| chr12:79863644
|
C | CA | 16 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(13): Show | 16 | HG00673.hp2 HG02074.hp1 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.368+9163dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863644 | ||||||
| chr12:79863644
|
CAAA | C | 9 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0233others(6): Show | 9 | HG00438.hp2 HG02145.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.368+9161_368+9163d others(5): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863644 | ||||||
| chr12:79863644
|
CAAAA | C | 108 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(105): Show | 109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.368+9160_368+9163d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863644 | ||||||
| chr12:79863644
|
CAAAAA | C | 99 | a0001c0001t0001g0130a0001c0001t0001g0245a0001c0001t0001g0253others(96): Show | 99 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.368+9159_368+9163d others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863644 | ||||||
| chr12:79863644
|
CAAAAAA | C | 7 | a0001c0001t0003g0182a0001c0002t0005g0003a0001c0002t0005g0112others(4): Show | 7 | HG00140.hp2 HG01109.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.368+9158_368+9163d others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863644 | ||||||
| chr12:79863644
|
CAAAAAAA others(10): Show |
C | 1 | a0002c0009t0005g0118 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.368+9147_368+9163d others(19): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863644 | ||||||
| chr12:79863832
|
C | T | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.368+8976G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863832 | ||||||
| chr12:79863861
|
G | C | 6 | a0001c0001t0004g0271a0001c0001t0004g0284a0001c0001t0004g0285others(3): Show | 6 | HG01243.hp2 HG01975.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.368+8947C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79863861 | ||||||
| chr12:79864242
|
G | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.368+8566C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79864242 | ||||||
| chr12:79864252
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.368+8556G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79864252 | ||||||
| chr12:79864342
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+8466C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79864342 | ||||||
| chr12:79864392
|
G | A | 1 | a0001c0002t0005g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.368+8416C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79864392 | ||||||
| chr12:79864521
|
A | G | 1 | a0001c0001t0004g0277 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.368+8287T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79864521 | ||||||
| chr12:79864542
|
A | G | 1 | a0001c0002t0002g0046 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.368+8266T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79864542 | ||||||
| chr12:79864544
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.368+8264C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79864544 | ||||||
| chr12:79865036
|
T | C | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.368+7772A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865036 | ||||||
| chr12:79865087
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+7721C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865087 | ||||||
| chr12:79865121
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.368+7687G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865121 | ||||||
| chr12:79865135
|
T | C | 120 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.368+7673A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865135 | ||||||
| chr12:79865263
|
C | T | 1 | a0001c0002t0006g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.368+7545G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865263 | ||||||
| chr12:79865312
|
C | T | 1 | a0001c0002t0009g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.368+7496G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865312 | ||||||
| chr12:79865336
|
T | C | 1 | a0001c0001t0004g0296 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.368+7472A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865336 | ||||||
| chr12:79865429
|
C | T | 1 | a0001c0001t0004g0295 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.368+7379G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865429 | ||||||
| chr12:79865446
|
A | G | 1 | a0001c0001t0004g0309 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.368+7362T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865446 | ||||||
| chr12:79865518
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+7290C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865518 | ||||||
| chr12:79865550
|
G | T | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.368+7258C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865550 | ||||||
| chr12:79865739
|
C | T | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.368+7069G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79865739 | ||||||
| chr12:79866111
|
C | G | 1 | a0001c0001t0003g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.368+6697G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79866111 | ||||||
| chr12:79866181
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.368+6627G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79866181 | ||||||
| chr12:79866300
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+6508G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79866300 | ||||||
| chr12:79866840
|
G | A | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+5968C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79866840 | ||||||
| chr12:79866889
|
A | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+5919T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79866889 | ||||||
| chr12:79866905
|
G | C | 2 | a0001c0001t0003g0145a0001c0001t0003g0146 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.368+5903C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79866905 | ||||||
| chr12:79867123
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+5685A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867123 | ||||||
| chr12:79867150
|
A | G | 1 | a0006c0007t0009g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.368+5658T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867150 | ||||||
| chr12:79867283
|
C | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.368+5525G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867283 | ||||||
| chr12:79867459
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.368+5349T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867459 | ||||||
| chr12:79867530
|
G | GAAAAAAG others(297): Show |
1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+5277_368+5278i others(306): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867530 | ||||||
| chr12:79867530
|
GA | G | 176 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(173): Show | 177 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.368+5277delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867530 | ||||||
| chr12:79867530
|
GAA | G | 11 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0300others(8): Show | 11 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.368+5276_368+5277d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867530 | ||||||
| chr12:79867840
|
C | G | 1 | a0001c0002t0005g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.368+4968G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867840 | ||||||
| chr12:79867923
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+4885C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867923 | ||||||
| chr12:79867937
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.368+4871C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867937 | ||||||
| chr12:79867952
|
A | C | 1 | a0006c0007t0009g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.368+4856T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867952 | ||||||
| chr12:79867963
|
G | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+4845C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79867963 | ||||||
| chr12:79868133
|
G | C | 1 | a0001c0001t0003g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368+4675C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868133 | ||||||
| chr12:79868209
|
T | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+4599A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868209 | ||||||
| chr12:79868305
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+4503C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868305 | ||||||
| chr12:79868342
|
T | C | 1 | a0001c0002t0002g0057 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.368+4466A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868342 | ||||||
| chr12:79868373
|
G | C | 14 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0177others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.368+4435C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868373 | ||||||
| chr12:79868454
|
A | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+4354T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868454 | ||||||
| chr12:79868568
|
G | GTAGATGG others(171): Show |
4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+4062_368+4239d others(180): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868568 | ||||||
| chr12:79868685
|
G | A | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | NA18950.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.368+4123C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868685 | ||||||
| chr12:79868730
|
G | C | 1 | a0001c0001t0004g0305 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.368+4078C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868730 | ||||||
| chr12:79868964
|
T | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+3844A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79868964 | ||||||
| chr12:79869315
|
G | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.368+3493C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869315 | ||||||
| chr12:79869422
|
A | G | 2 | a0001c0002t0005g0123a0001c0002t0005g0124 | 2 | HG02572.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.368+3386T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869422 | ||||||
| chr12:79869455
|
C | A | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+3353G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869455 | ||||||
| chr12:79869617
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.368+3191G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869617 | ||||||
| chr12:79869694
|
G | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.368+3114C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869694 | ||||||
| chr12:79869903
|
C | CTAT | 21 | a0001c0001t0001g0188a0001c0001t0001g0233a0001c0001t0001g0234others(18): Show | 21 | HG02717.hp1 HG03098.hp1 HG03098.hp2 others(18): Show |
intron_variant | MODIFIER | c.368+2902_368+2904d others(5): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869903 | ||||||
| chr12:79869903
|
C | CTATTAT | 63 | a0001c0001t0003g0133a0001c0001t0004g0001a0001c0001t0004g0267others(60): Show | 64 | HG00140.hp2 HG00408.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.368+2899_368+2904d others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869903 | ||||||
| chr12:79869903
|
C | CTATTATT others(2): Show |
23 | a0001c0001t0003g0264a0001c0001t0004g0278a0001c0001t0004g0279others(20): Show | 23 | HG01074.hp2 HG01109.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.368+2896_368+2904d others(11): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869903 | ||||||
| chr12:79869903
|
C | CTATTATT others(5): Show |
4 | a0001c0002t0008g0090a0001c0002t0009g0012a0001c0002t0010g0009others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+2893_368+2904d others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869903 | ||||||
| chr12:79869903
|
CTAT | C | 6 | a0001c0002t0006g0005a0001c0002t0006g0033a0001c0002t0006g0034others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+2902_368+2904d others(5): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869903 | ||||||
| chr12:79869994
|
A | G | 2 | a0001c0001t0003g0144a0001c0001t0003g0147 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.368+2814T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79869994 | ||||||
| chr12:79870177
|
C | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+2631G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79870177 | ||||||
| chr12:79870200
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368+2608C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79870200 | ||||||
| chr12:79870335
|
C | T | 1 | a0001c0001t0012g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.368+2473G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79870335 | ||||||
| chr12:79870463
|
C | T | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.368+2345G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79870463 | ||||||
| chr12:79870485
|
T | C | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.368+2323A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79870485 | ||||||
| chr12:79870542
|
G | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.368+2266C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79870542 | ||||||
| chr12:79870664
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.368+2144G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79870664 | ||||||
| chr12:79870798
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.368+2010G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79870798 | ||||||
| chr12:79871342
|
G | C | 1 | a0001c0002t0002g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.368+1466C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79871342 | ||||||
| chr12:79871375
|
G | T | 1 | a0001c0001t0003g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.368+1433C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79871375 | ||||||
| chr12:79871517
|
A | G | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.368+1291T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79871517 | ||||||
| chr12:79871666
|
G | A | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.368+1142C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79871666 | ||||||
| chr12:79871854
|
G | A | 1 | a0001c0002t0005g0125 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.368+954C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79871854 | ||||||
| chr12:79872042
|
G | A | 6 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0303others(3): Show | 6 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.368+766C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79872042 | ||||||
| chr12:79872050
|
A | G | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.368+758T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79872050 | ||||||
| chr12:79872581
|
A | T | 1 | a0001c0001t0001g0251 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.368+227T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79872581 | ||||||
| chr12:79872592
|
G | A | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.368+216C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79872592 | ||||||
| chr12:79872699
|
C | T | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.368+109G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79872699 | ||||||
| chr12:79872743
|
C | T | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.368+65G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 2/24 | chr12 | 79872743 | ||||||
| chr12:79873461
|
A | T | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.238-523T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79873461 | ||||||
| chr12:79873496
|
T | TA | 194 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(191): Show | 195 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.238-559dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79873496 | ||||||
| chr12:79873496
|
T | TAA | 6 | a0001c0001t0001g0215a0001c0001t0004g0277a0001c0002t0006g0033others(3): Show | 6 | HG01074.hp2 HG03490.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-560_238-559dup others(2): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79873496 | ||||||
| chr12:79873509
|
A | C | 5 | a0001c0002t0002g0015a0001c0002t0002g0021a0001c0002t0002g0022others(2): Show | 5 | HG00438.hp1 HG02040.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-571T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79873509 | ||||||
| chr12:79873572
|
A | T | 1 | a0001c0002t0008g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.238-634T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79873572 | ||||||
| chr12:79873727
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-789T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79873727 | ||||||
| chr12:79873785
|
A | T | 4 | a0001c0001t0004g0001a0001c0001t0004g0273a0001c0001t0004g0276others(1): Show | 5 | NA18956.hp1 NA18964.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-847T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79873785 | ||||||
| chr12:79874042
|
G | A | 1 | a0001c0001t0004g0303 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.238-1104C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79874042 | ||||||
| chr12:79874113
|
T | G | 1 | a0001c0001t0003g0179 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.238-1175A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79874113 | ||||||
| chr12:79874235
|
T | C | 1 | a0006c0007t0009g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.238-1297A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79874235 | ||||||
| chr12:79874522
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.238-1584G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79874522 | ||||||
| chr12:79874605
|
G | A | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.238-1667C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79874605 | ||||||
| chr12:79874655
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.238-1717T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79874655 | ||||||
| chr12:79875023
|
C | A | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.238-2085G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875023 | ||||||
| chr12:79875144
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.238-2206A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875144 | ||||||
| chr12:79875179
|
A | G | 1 | a0001c0002t0005g0121 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238-2241T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875179 | ||||||
| chr12:79875289
|
T | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0226 | 2 | HG00639.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.238-2351A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875289 | ||||||
| chr12:79875456
|
C | T | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.238-2518G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875456 | ||||||
| chr12:79875465
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.238-2527A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875465 | ||||||
| chr12:79875489
|
G | C | 1 | a0001c0001t0003g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.238-2551C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875489 | ||||||
| chr12:79875604
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-2666A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875604 | ||||||
| chr12:79875685
|
A | G | 70 | a0001c0001t0001g0127a0001c0001t0001g0194a0001c0001t0001g0195others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.238-2747T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875685 | ||||||
| chr12:79875890
|
A | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.238-2952T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875890 | ||||||
| chr12:79875966
|
G | A | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.238-3028C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79875966 | ||||||
| chr12:79876006
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.238-3068A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79876006 | ||||||
| chr12:79876158
|
G | T | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-3220C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79876158 | ||||||
| chr12:79876551
|
T | G | 1 | a0001c0002t0005g0124 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.238-3613A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79876551 | ||||||
| chr12:79876686
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.238-3748A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79876686 | ||||||
| chr12:79876812
|
C | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3874G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79876812 | ||||||
| chr12:79876869
|
C | T | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.238-3931G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79876869 | ||||||
| chr12:79876935
|
C | T | 1 | a0001c0001t0019g0272 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.238-3997G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79876935 | ||||||
| chr12:79877012
|
G | GA | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.238-4075dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877012 | ||||||
| chr12:79877079
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-4141A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877079 | ||||||
| chr12:79877115
|
T | C | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-4177A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877115 | ||||||
| chr12:79877127
|
T | C | 1 | a0001c0002t0002g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.238-4189A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877127 | ||||||
| chr12:79877289
|
C | G | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.238-4351G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877289 | ||||||
| chr12:79877481
|
C | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.238-4543G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877481 | ||||||
| chr12:79877582
|
C | T | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.238-4644G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877582 | ||||||
| chr12:79877608
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.238-4670G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877608 | ||||||
| chr12:79877824
|
T | C | 1 | a0001c0001t0003g0189 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.238-4886A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877824 | ||||||
| chr12:79877825
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.238-4887A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79877825 | ||||||
| chr12:79878054
|
T | G | 29 | a0001c0002t0005g0002a0001c0002t0005g0099a0001c0002t0005g0100others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.238-5116A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79878054 | ||||||
| chr12:79878091
|
C | T | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-5153G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79878091 | ||||||
| chr12:79878131
|
C | A | 1 | a0001c0001t0004g0308 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.238-5193G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79878131 | ||||||
| chr12:79878210
|
T | TA | 122 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(119): Show | 122 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.238-5273dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79878210 | ||||||
| chr12:79878382
|
T | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-5444A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79878382 | ||||||
| chr12:79878409
|
G | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-5471C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79878409 | ||||||
| chr12:79878457
|
G | A | 2 | a0001c0002t0005g0100a0001c0002t0005g0110 | 2 | HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.238-5519C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79878457 | ||||||
| chr12:79878678
|
C | T | 2 | a0001c0002t0002g0042a0001c0002t0002g0048 | 2 | HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.238-5740G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79878678 | ||||||
| chr12:79879250
|
C | T | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238-6312G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79879250 | ||||||
| chr12:79879466
|
C | G | 235 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.238-6528G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79879466 | ||||||
| chr12:79880059
|
G | A | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.238-7121C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880059 | ||||||
| chr12:79880107
|
A | G | 1 | a0001c0001t0004g0305 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.238-7169T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880107 | ||||||
| chr12:79880109
|
A | G | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-7171T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880109 | ||||||
| chr12:79880129
|
G | A | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238-7191C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880129 | ||||||
| chr12:79880293
|
A | G | 1 | a0001c0002t0002g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.238-7355T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880293 | ||||||
| chr12:79880332
|
A | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-7394T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880332 | ||||||
| chr12:79880387
|
TAAAC | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-7453_238-7450d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880387 | ||||||
| chr12:79880393
|
A | G | 15 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0100others(12): Show | 15 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-7455T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880393 | ||||||
| chr12:79880394
|
A | T | 15 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0100others(12): Show | 15 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-7456T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880394 | ||||||
| chr12:79880561
|
C | T | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.238-7623G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880561 | ||||||
| chr12:79880783
|
TTTTG | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.238-7849_238-7846d others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79880783 | ||||||
| chr12:79881030
|
T | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-8092A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79881030 | ||||||
| chr12:79881195
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-8257A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79881195 | ||||||
| chr12:79881403
|
G | C | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.238-8465C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79881403 | ||||||
| chr12:79881669
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0216 | 2 | NA18747.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.238-8731G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79881669 | ||||||
| chr12:79881697
|
A | G | 1 | a0001c0001t0003g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.238-8759T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79881697 | ||||||
| chr12:79881707
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-8769T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79881707 | ||||||
| chr12:79881876
|
T | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-8938A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79881876 | ||||||
| chr12:79881988
|
C | T | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-9050G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79881988 | ||||||
| chr12:79882066
|
G | C | 1 | a0001c0002t0002g0004 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.238-9128C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882066 | ||||||
| chr12:79882088
|
G | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-9150C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882088 | ||||||
| chr12:79882227
|
G | A | 1 | a0001c0002t0002g0058 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.238-9289C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882227 | ||||||
| chr12:79882357
|
C | T | 37 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0003g0006others(34): Show | 37 | HG00408.hp2 HG00544.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.238-9419G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882357 | ||||||
| chr12:79882583
|
T | C | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-9645A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882583 | ||||||
| chr12:79882620
|
C | A | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | NA18950.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.238-9682G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882620 | ||||||
| chr12:79882713
|
C | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-9775G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882713 | ||||||
| chr12:79882726
|
T | C | 1 | a0001c0002t0005g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.238-9788A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882726 | ||||||
| chr12:79882785
|
C | T | 1 | a0001c0002t0009g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.238-9847G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882785 | ||||||
| chr12:79882878
|
C | T | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-9940G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882878 | ||||||
| chr12:79882905
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.238-9967C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882905 | ||||||
| chr12:79882909
|
C | T | 68 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0003g0006others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.238-9971G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882909 | ||||||
| chr12:79882929
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.238-9991C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79882929 | ||||||
| chr12:79883007
|
C | T | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-10069G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883007 | ||||||
| chr12:79883022
|
A | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-10084T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883022 | ||||||
| chr12:79883030
|
G | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-10092C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883030 | ||||||
| chr12:79883047
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0226 | 2 | HG00639.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.238-10109C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883047 | ||||||
| chr12:79883090
|
T | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-10152A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883090 | ||||||
| chr12:79883113
|
G | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-10175C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883113 | ||||||
| chr12:79883116
|
G | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.238-10178C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883116 | ||||||
| chr12:79883131
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-10193G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883131 | ||||||
| chr12:79883269
|
C | CATT | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.238-10334_238-1033 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883269 | ||||||
| chr12:79883364
|
A | C | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-10426T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883364 | ||||||
| chr12:79883498
|
T | G | 1 | a0001c0002t0006g0081 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.238-10560A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883498 | ||||||
| chr12:79883537
|
C | T | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-10599G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883537 | ||||||
| chr12:79883573
|
AATTTT | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.238-10640_238-1063 others(9): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883573 | ||||||
| chr12:79883663
|
A | G | 1 | a0001c0001t0003g0169 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.238-10725T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883663 | ||||||
| chr12:79883692
|
T | C | 2 | a0001c0001t0004g0268a0001c0001t0004g0269 | 2 | HG00408.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.238-10754A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883692 | ||||||
| chr12:79883796
|
T | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-10858A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883796 | ||||||
| chr12:79883836
|
G | T | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.238-10898C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883836 | ||||||
| chr12:79883940
|
C | T | 3 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0019 | 3 | NA18944.hp1 NA18947.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.238-11002G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79883940 | ||||||
| chr12:79884678
|
C | G | 1 | a0001c0001t0003g0174 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.238-11740G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79884678 | ||||||
| chr12:79884684
|
T | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.238-11746A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79884684 | ||||||
| chr12:79884861
|
T | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-11923A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79884861 | ||||||
| chr12:79885178
|
C | T | 1 | a0001c0002t0005g0123 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.238-12240G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79885178 | ||||||
| chr12:79885299
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-12361T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79885299 | ||||||
| chr12:79885322
|
A | C | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.238-12384T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79885322 | ||||||
| chr12:79885821
|
G | A | 1 | a0001c0001t0004g0277 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.238-12883C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79885821 | ||||||
| chr12:79885871
|
T | C | 1 | a0001c0001t0004g0294 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.238-12933A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79885871 | ||||||
| chr12:79886024
|
C | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-13086G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79886024 | ||||||
| chr12:79886354
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.238-13416T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79886354 | ||||||
| chr12:79886469
|
T | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-13531A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79886469 | ||||||
| chr12:79886630
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.238-13692T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79886630 | ||||||
| chr12:79886882
|
C | T | 2 | a0001c0002t0010g0008a0001c0002t0010g0009 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.238-13944G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79886882 | ||||||
| chr12:79886940
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-14002T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79886940 | ||||||
| chr12:79887064
|
G | C | 187 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(184): Show | 188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.238-14126C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887064 | ||||||
| chr12:79887321
|
T | TTA | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.238-14385_238-1438 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887321 | ||||||
| chr12:79887378
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-14440T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887378 | ||||||
| chr12:79887512
|
C | T | 1 | a0001c0002t0002g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.238-14574G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887512 | ||||||
| chr12:79887538
|
T | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-14600A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887538 | ||||||
| chr12:79887601
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-14663G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887601 | ||||||
| chr12:79887604
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0254 | 2 | NA19078.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.238-14666C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887604 | ||||||
| chr12:79887660
|
G | A | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.238-14722C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887660 | ||||||
| chr12:79887673
|
T | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0247 | 2 | NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.238-14735A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887673 | ||||||
| chr12:79887723
|
G | A | 1 | a0001c0001t0011g0304 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.238-14785C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887723 | ||||||
| chr12:79887779
|
A | G | 1 | a0001c0002t0005g0108 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.238-14841T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887779 | ||||||
| chr12:79887990
|
A | G | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-15052T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79887990 | ||||||
| chr12:79888292
|
G | C | 1 | a0001c0002t0005g0123 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.238-15354C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79888292 | ||||||
| chr12:79888591
|
T | TTCCTAGT others(10): Show |
38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.238-15670_238-1565 others(21): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79888591 | ||||||
| chr12:79888705
|
T | G | 1 | a0005c0005t0003g0185 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.238-15767A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79888705 | ||||||
| chr12:79889333
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-16395G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79889333 | ||||||
| chr12:79889385
|
C | T | 2 | a0001c0001t0004g0001a0001c0001t0004g0283 | 3 | NA18964.hp1 NA19064.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.238-16447G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79889385 | ||||||
| chr12:79889413
|
G | A | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-16475C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79889413 | ||||||
| chr12:79889925
|
G | C | 1 | a0001c0002t0002g0057 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.238-16987C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79889925 | ||||||
| chr12:79890223
|
A | G | 12 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0300others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.238-17285T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890223 | ||||||
| chr12:79890230
|
A | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-17292T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890230 | ||||||
| chr12:79890265
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-17327C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890265 | ||||||
| chr12:79890322
|
G | C | 3 | a0001c0002t0002g0043a0001c0002t0002g0049a0001c0002t0002g0059 | 3 | NA18747.hp2 NA18993.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.238-17384C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890322 | ||||||
| chr12:79890701
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-17763G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890701 | ||||||
| chr12:79890734
|
TAA | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02683.hp1 HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.238-17798_238-1779 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890734 | ||||||
| chr12:79890887
|
CCACCCAC others(3): Show |
C | 4 | a0001c0002t0005g0122a0001c0002t0009g0010a0001c0002t0009g0011others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-17959_238-1795 others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890887 | ||||||
| chr12:79890889
|
ACC | A | 5 | a0001c0002t0006g0029a0001c0002t0006g0033a0001c0002t0006g0080others(2): Show | 5 | HG03710.hp2 NA18990.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-17953_238-1795 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890889 | ||||||
| chr12:79890889
|
ACCCACCC others(9): Show |
A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-17967_238-1795 others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890889 | ||||||
| chr12:79890891
|
C | A | 4 | a0001c0001t0003g0146a0001c0002t0006g0079a0001c0002t0006g0084others(1): Show | 4 | HG03831.hp1 HG06807.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-17953G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890891 | ||||||
| chr12:79890891
|
CCACCCAC others(9): Show |
C | 3 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009 | 3 | HG02055.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.238-17969_238-1795 others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890891 | ||||||
| chr12:79890893
|
ACCCACAC others(5): Show |
A | 5 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-17967_238-1795 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890893 | ||||||
| chr12:79890895
|
C | A | 12 | a0001c0001t0001g0202a0001c0002t0006g0029a0001c0002t0006g0033others(9): Show | 12 | HG03710.hp2 HG03831.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.238-17957G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890895 | ||||||
| chr12:79890895
|
CCACACCC others(5): Show |
C | 6 | a0001c0002t0005g0119a0001c0002t0005g0120a0001c0002t0009g0092others(3): Show | 6 | HG01074.hp2 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-17969_238-1795 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890895 | ||||||
| chr12:79890895
|
CCACACCC others(7): Show |
C | 7 | a0001c0002t0005g0121a0001c0002t0005g0125a0001c0002t0008g0095others(4): Show | 7 | HG01243.hp1 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-17971_238-1795 others(18): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890895 | ||||||
| chr12:79890895
|
CCACACCC others(9): Show |
C | 6 | a0001c0002t0002g0020a0001c0002t0002g0046a0001c0002t0008g0087others(3): Show | 6 | HG02056.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-17973_238-1795 others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890895 | ||||||
| chr12:79890897
|
ACACC | A | 10 | a0001c0001t0003g0166a0001c0002t0002g0025a0001c0002t0002g0028others(7): Show | 10 | HG01192.hp1 HG01261.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.238-17963_238-1796 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890897 | ||||||
| chr12:79890897
|
ACACCCAC others(1): Show |
A | 21 | a0001c0002t0002g0017a0001c0002t0002g0044a0001c0002t0005g0002others(18): Show | 21 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.238-17967_238-1796 others(12): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890897 | ||||||
| chr12:79890899
|
ACC | A | 40 | a0001c0001t0003g0146a0001c0002t0002g0013a0001c0002t0002g0015others(37): Show | 40 | HG00423.hp1 HG00673.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.238-17963_238-1796 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890899 | ||||||
| chr12:79890899
|
ACCCACC | A | 5 | a0001c0001t0001g0202a0001c0002t0002g0057a0001c0002t0005g0102others(2): Show | 5 | HG02280.hp2 HG03195.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-17967_238-1796 others(10): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890899 | ||||||
| chr12:79890901
|
C | A | 21 | a0001c0001t0003g0132a0001c0001t0003g0149a0001c0002t0002g0004others(18): Show | 21 | HG00438.hp1 HG00597.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.238-17963G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890901 | ||||||
| chr12:79890901
|
C | CCA | 25 | a0001c0001t0003g0133a0001c0001t0003g0155a0001c0001t0003g0156others(22): Show | 25 | HG00741.hp2 HG02074.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.238-17965_238-1796 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890901 | ||||||
| chr12:79890901
|
C | CCACA | 14 | a0001c0001t0001g0218a0001c0001t0001g0231a0001c0001t0001g0246others(11): Show | 14 | HG00639.hp1 HG01256.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.238-17964_238-1796 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890901 | ||||||
| chr12:79890901
|
C | CCACACA | 12 | a0001c0001t0001g0226a0001c0001t0003g0128a0001c0001t0004g0298others(9): Show | 12 | HG00639.hp2 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-17964_238-1796 others(10): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890901 | ||||||
| chr12:79890903
|
ACC | A | 39 | a0001c0001t0001g0130a0001c0001t0003g0158a0001c0001t0003g0174others(36): Show | 40 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.238-17967_238-1796 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890903 | ||||||
| chr12:79890905
|
C | A | 136 | a0001c0001t0001g0218a0001c0001t0001g0226a0001c0001t0001g0231others(133): Show | 136 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.238-17967G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890905 | ||||||
| chr12:79890905
|
C | CCA | 7 | a0001c0001t0001g0235a0001c0001t0001g0239a0001c0001t0007g0134others(4): Show | 7 | HG01496.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-17969_238-1796 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890905 | ||||||
| chr12:79890905
|
C | CCACA | 15 | a0001c0001t0001g0194a0001c0001t0001g0203a0001c0001t0001g0205others(12): Show | 15 | HG00438.hp2 HG01168.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.238-17971_238-1796 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890905 | ||||||
| chr12:79890905
|
C | CCACACA | 37 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0195others(34): Show | 37 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.238-17973_238-1796 others(10): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890905 | ||||||
| chr12:79890905
|
C | CCACACAC others(1): Show |
8 | a0001c0001t0001g0196a0001c0001t0001g0221a0001c0001t0001g0228others(5): Show | 8 | HG01074.hp1 HG01261.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-17975_238-1796 others(12): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890905 | ||||||
| chr12:79890905
|
C | CCACACAC others(3): Show |
4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0240others(1): Show | 4 | HG01934.hp1 HG02027.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-17977_238-1796 others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890905 | ||||||
| chr12:79890951
|
ACTCT | A | 7 | a0001c0001t0004g0280a0001c0001t0004g0281a0001c0001t0020g0310others(4): Show | 7 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-18017_238-1801 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79890951 | ||||||
| chr12:79891109
|
G | A | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.238-18171C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79891109 | ||||||
| chr12:79891127
|
G | C | 1 | a0001c0006t0002g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.238-18189C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79891127 | ||||||
| chr12:79891164
|
A | T | 47 | a0001c0001t0004g0001a0001c0001t0004g0267a0001c0001t0004g0268others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.238-18226T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79891164 | ||||||
| chr12:79891174
|
A | T | 1 | a0001c0001t0003g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.238-18236T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79891174 | ||||||
| chr12:79891757
|
C | T | 2 | a0001c0002t0006g0075a0001c0002t0006g0082 | 2 | NA19060.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.238-18819G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79891757 | ||||||
| chr12:79892125
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-19187T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892125 | ||||||
| chr12:79892243
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | NA18977.hp2 NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.238-19305A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892243 | ||||||
| chr12:79892247
|
T | C | 1 | a0001c0002t0005g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238-19309A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892247 | ||||||
| chr12:79892293
|
A | T | 2 | a0001c0002t0006g0076a0001c0002t0006g0077 | 2 | NA18981.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.238-19355T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892293 | ||||||
| chr12:79892297
|
C | T | 2 | a0001c0002t0006g0076a0001c0002t0006g0077 | 2 | NA18981.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.238-19359G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892297 | ||||||
| chr12:79892399
|
C | T | 123 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(120): Show | 123 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.238-19461G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892399 | ||||||
| chr12:79892680
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-19742C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892680 | ||||||
| chr12:79892713
|
G | C | 2 | a0001c0001t0004g0282a0001c0001t0018g0266 | 2 | NA18990.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.238-19775C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892713 | ||||||
| chr12:79892743
|
T | G | 1 | a0001c0001t0007g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238-19805A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892743 | ||||||
| chr12:79892757
|
TC | T | 26 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(23): Show | 26 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.238-19820delG | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892757 | ||||||
| chr12:79892801
|
A | T | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.238-19863T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892801 | ||||||
| chr12:79892852
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.238-19914G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892852 | ||||||
| chr12:79892886
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.238-19948A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892886 | ||||||
| chr12:79892933
|
G | A | 1 | a0001c0001t0004g0290 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.238-19995C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79892933 | ||||||
| chr12:79893029
|
G | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.238-20091C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79893029 | ||||||
| chr12:79893104
|
C | CA | 10 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0004g0283others(7): Show | 10 | HG00741.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.238-20167dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79893104 | ||||||
| chr12:79893257
|
C | T | 253 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(250): Show | 254 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.238-20319G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79893257 | ||||||
| chr12:79893348
|
T | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG00438.hp2 HG03834.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-20410A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79893348 | ||||||
| chr12:79893725
|
C | T | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238-20787G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79893725 | ||||||
| chr12:79893754
|
A | T | 1 | a0001c0002t0002g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.238-20816T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79893754 | ||||||
| chr12:79894042
|
C | T | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.238-21104G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79894042 | ||||||
| chr12:79894080
|
T | C | 1 | a0001c0002t0005g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.238-21142A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79894080 | ||||||
| chr12:79894123
|
A | G | 12 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0300others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.238-21185T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79894123 | ||||||
| chr12:79894126
|
A | G | 1 | a0001c0001t0004g0274 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.238-21188T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79894126 | ||||||
| chr12:79894387
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.238-21449C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79894387 | ||||||
| chr12:79894874
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-21936G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79894874 | ||||||
| chr12:79894919
|
C | A | 3 | a0001c0001t0003g0162a0001c0001t0003g0168a0001c0001t0003g0169 | 3 | HG02074.hp2 NA18993.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.238-21981G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79894919 | ||||||
| chr12:79895071
|
G | A | 2 | a0001c0002t0005g0099a0002c0009t0005g0118 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.238-22133C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79895071 | ||||||
| chr12:79895530
|
GCAATGTA others(7): Show |
G | 66 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0003g0006others(63): Show | 66 | HG00408.hp2 HG00544.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.238-22606_238-2259 others(18): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79895530 | ||||||
| chr12:79895532
|
AATGTATA others(4): Show |
A | 2 | a0001c0001t0003g0144a0001c0001t0003g0191 | 2 | HG00639.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.238-22605_238-2259 others(15): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79895532 | ||||||
| chr12:79895544
|
T | G | 2 | a0001c0001t0003g0144a0001c0001t0003g0191 | 2 | HG00639.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.238-22606A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79895544 | ||||||
| chr12:79895621
|
T | C | 1 | a0001c0002t0005g0112 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.238-22683A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79895621 | ||||||
| chr12:79895779
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-22841C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79895779 | ||||||
| chr12:79895885
|
C | T | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | NA18950.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.238-22947G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79895885 | ||||||
| chr12:79895893
|
G | A | 1 | a0001c0002t0002g0022 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.238-22955C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79895893 | ||||||
| chr12:79896002
|
AT | A | 138 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(135): Show | 138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.238-23065delA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896002 | ||||||
| chr12:79896013
|
T | A | 2 | a0001c0001t0004g0299a0001c0001t0019g0272 | 2 | HG02015.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.238-23075A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896013 | ||||||
| chr12:79896017
|
AGAG | A | 45 | a0001c0001t0004g0001a0001c0001t0004g0267a0001c0001t0004g0268others(42): Show | 46 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.238-23082_238-2308 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896017 | ||||||
| chr12:79896285
|
C | A | 1 | a0001c0002t0006g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.238-23347G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896285 | ||||||
| chr12:79896421
|
C | A | 1 | a0001c0001t0003g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.238-23483G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896421 | ||||||
| chr12:79896578
|
C | T | 1 | a0001c0002t0002g0049 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.238-23640G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896578 | ||||||
| chr12:79896609
|
G | A | 51 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0003g0006others(48): Show | 51 | HG00408.hp2 HG00544.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.238-23671C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896609 | ||||||
| chr12:79896681
|
G | C | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-23743C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896681 | ||||||
| chr12:79896907
|
T | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-23969A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79896907 | ||||||
| chr12:79897034
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0263 | 2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.238-24096G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79897034 | ||||||
| chr12:79897092
|
T | C | 1 | a0001c0002t0005g0123 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.238-24154A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79897092 | ||||||
| chr12:79897224
|
T | C | 1 | a0001c0001t0004g0307 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.238-24286A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79897224 | ||||||
| chr12:79897246
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.238-24308C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79897246 | ||||||
| chr12:79897326
|
A | T | 2 | a0001c0002t0005g0119a0001c0002t0005g0120 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.238-24388T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79897326 | ||||||
| chr12:79897708
|
C | T | 7 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0112others(4): Show | 7 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-24770G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79897708 | ||||||
| chr12:79898024
|
C | G | 16 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0003g0006others(13): Show | 16 | HG00408.hp2 HG00544.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.238-25086G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79898024 | ||||||
| chr12:79898381
|
G | A | 30 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.238-25443C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79898381 | ||||||
| chr12:79898591
|
T | G | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-25653A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79898591 | ||||||
| chr12:79898908
|
T | C | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.238-25970A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79898908 | ||||||
| chr12:79899158
|
CATTA | C | 138 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(135): Show | 138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.238-26224_238-2622 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899158 | ||||||
| chr12:79899233
|
A | AAT | 7 | a0001c0002t0002g0042a0001c0002t0002g0044a0001c0002t0002g0049others(4): Show | 7 | HG01099.hp2 HG02074.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-26297_238-2629 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
A | AATAT | 3 | a0001c0002t0002g0048a0001c0002t0002g0063a0001c0002t0002g0072 | 3 | HG03239.hp1 HG03927.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.238-26299_238-2629 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
A | AATATATA others(3): Show |
1 | a0001c0002t0002g0047 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.238-26305_238-2629 others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AAT | A | 7 | a0001c0002t0002g0023a0001c0002t0002g0043a0001c0002t0002g0054others(4): Show | 7 | HG00673.hp2 HG02027.hp1 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-26297_238-2629 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATAT | A | 14 | a0001c0002t0002g0015a0001c0002t0002g0020a0001c0002t0002g0025others(11): Show | 14 | HG01943.hp1 HG02040.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.238-26299_238-2629 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATAT | A | 4 | a0001c0002t0002g0024a0001c0002t0002g0038a0001c0002t0002g0046others(1): Show | 4 | HG00438.hp1 HG02056.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-26301_238-2629 others(10): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(1): Show |
A | 5 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0019others(2): Show | 5 | HG00423.hp1 NA18944.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-26303_238-2629 others(12): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(3): Show |
A | 1 | a0001c0002t0009g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.238-26305_238-2629 others(14): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(5): Show |
A | 3 | a0001c0002t0002g0039a0001c0002t0006g0076a0001c0002t0009g0012 | 3 | HG03041.hp2 NA18981.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.238-26307_238-2629 others(16): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(7): Show |
A | 2 | a0001c0002t0006g0077a0001c0002t0009g0010 | 2 | HG02559.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.238-26309_238-2629 others(18): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(9): Show |
A | 2 | a0001c0002t0006g0037a0001c0002t0006g0078 | 2 | HG02886.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.238-26311_238-2629 others(20): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(11): Show |
A | 7 | a0001c0002t0002g0004a0001c0002t0006g0005a0001c0002t0006g0030others(4): Show | 7 | HG00597.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-26313_238-2629 others(22): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(13): Show |
A | 8 | a0001c0002t0006g0029a0001c0002t0006g0033a0001c0002t0006g0036others(5): Show | 8 | HG03130.hp1 HG03710.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-26315_238-2629 others(24): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(15): Show |
A | 5 | a0001c0002t0005g0122a0001c0002t0010g0007a0001c0002t0010g0008others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-26317_238-2629 others(26): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(17): Show |
A | 2 | a0001c0002t0002g0062a0001c0002t0005g0106 | 2 | HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.238-26319_238-2629 others(28): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(19): Show |
A | 32 | a0001c0001t0001g0232a0001c0001t0003g0150a0001c0001t0004g0276others(29): Show | 32 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.238-26321_238-2629 others(30): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(21): Show |
A | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.238-26323_238-2629 others(32): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899233
|
AATATATA others(23): Show |
A | 4 | a0001c0001t0003g0189a0001c0002t0009g0092a0001c0002t0009g0093others(1): Show | 4 | HG01074.hp2 NA18906.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-26325_238-2629 others(34): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899233 | ||||||
| chr12:79899257
|
T | A | 3 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009 | 3 | HG02055.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.238-26319A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899257 | ||||||
| chr12:79899259
|
T | A | 2 | a0001c0002t0010g0008a0001c0002t0010g0009 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.238-26321A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899259 | ||||||
| chr12:79899435
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.238-26497G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899435 | ||||||
| chr12:79899728
|
C | G | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.238-26790G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79899728 | ||||||
| chr12:79900107
|
C | T | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.238-27169G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900107 | ||||||
| chr12:79900195
|
A | T | 1 | a0001c0002t0006g0078 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.238-27257T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900195 | ||||||
| chr12:79900243
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-27305G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900243 | ||||||
| chr12:79900467
|
C | T | 1 | a0004c0004t0005g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.238-27529G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900467 | ||||||
| chr12:79900710
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG00140.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.238-27772C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900710 | ||||||
| chr12:79900721
|
G | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-27783C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900721 | ||||||
| chr12:79900732
|
CTAAA | C | 4 | a0001c0001t0004g0284a0001c0002t0002g0045a0001c0002t0002g0066others(1): Show | 4 | NA18966.hp2 NA18999.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-27798_238-2779 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900732 | ||||||
| chr12:79900874
|
G | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.238-27936C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900874 | ||||||
| chr12:79900907
|
C | T | 1 | a0001c0002t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.238-27969G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900907 | ||||||
| chr12:79900934
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.238-27996G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79900934 | ||||||
| chr12:79901384
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.238-28446C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79901384 | ||||||
| chr12:79901684
|
C | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0245 | 2 | HG02027.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.238-28746G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79901684 | ||||||
| chr12:79901693
|
T | G | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-28755A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79901693 | ||||||
| chr12:79901784
|
G | A | 1 | a0001c0002t0006g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.238-28846C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79901784 | ||||||
| chr12:79901829
|
T | C | 1 | a0001c0002t0009g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.238-28891A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79901829 | ||||||
| chr12:79901914
|
T | C | 1 | a0001c0001t0003g0183 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.238-28976A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79901914 | ||||||
| chr12:79902040
|
C | T | 9 | a0001c0001t0004g0271a0001c0001t0004g0284a0001c0001t0004g0285others(6): Show | 9 | HG01243.hp2 HG01975.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.238-29102G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902040 | ||||||
| chr12:79902058
|
G | A | 1 | a0001c0001t0003g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.238-29120C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902058 | ||||||
| chr12:79902059
|
A | T | 12 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0300others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.238-29121T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902059 | ||||||
| chr12:79902239
|
A | C | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-29301T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902239 | ||||||
| chr12:79902332
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.238-29394C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902332 | ||||||
| chr12:79902347
|
T | C | 4 | a0001c0002t0005g0113a0001c0002t0005g0114a0001c0002t0005g0115others(1): Show | 4 | HG00140.hp2 HG01109.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-29409A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902347 | ||||||
| chr12:79902613
|
G | A | 1 | a0001c0001t0003g0169 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.238-29675C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902613 | ||||||
| chr12:79902798
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.238-29860C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902798 | ||||||
| chr12:79902832
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.238-29894T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902832 | ||||||
| chr12:79902882
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-29944T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902882 | ||||||
| chr12:79902946
|
C | T | 1 | a0001c0002t0002g0020 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.238-30008G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79902946 | ||||||
| chr12:79903016
|
T | TTATC | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-30082_238-3007 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903016 | ||||||
| chr12:79903096
|
G | A | 1 | a0001c0001t0003g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.238-30158C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903096 | ||||||
| chr12:79903174
|
G | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-30236C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903174 | ||||||
| chr12:79903191
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-30253A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903191 | ||||||
| chr12:79903257
|
C | T | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-30319G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903257 | ||||||
| chr12:79903319
|
C | G | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG00438.hp2 HG03834.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-30381G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903319 | ||||||
| chr12:79903450
|
C | CA | 166 | a0001c0001t0001g0225a0001c0001t0001g0239a0001c0001t0004g0001others(163): Show | 167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.238-30513dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903450 | ||||||
| chr12:79903685
|
T | A | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.238-30747A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903685 | ||||||
| chr12:79903692
|
A | G | 3 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0013g0089 | 3 | HG02280.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.238-30754T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903692 | ||||||
| chr12:79903700
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238-30762G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903700 | ||||||
| chr12:79903779
|
T | C | 1 | a0001c0002t0005g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.238-30841A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903779 | ||||||
| chr12:79903877
|
T | C | 1 | a0001c0002t0002g0043 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.237+30818A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903877 | ||||||
| chr12:79903890
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+30805A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903890 | ||||||
| chr12:79903918
|
C | T | 124 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(121): Show | 124 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.237+30777G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79903918 | ||||||
| chr12:79904071
|
C | A | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+30624G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904071 | ||||||
| chr12:79904139
|
C | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.237+30556G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904139 | ||||||
| chr12:79904224
|
A | G | 3 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0019 | 3 | NA18944.hp1 NA18947.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.237+30471T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904224 | ||||||
| chr12:79904231
|
T | C | 1 | a0001c0002t0002g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.237+30464A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904231 | ||||||
| chr12:79904259
|
T | C | 1 | a0004c0004t0005g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.237+30436A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904259 | ||||||
| chr12:79904329
|
A | C | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.237+30366T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904329 | ||||||
| chr12:79904400
|
G | C | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+30295C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904400 | ||||||
| chr12:79904548
|
T | A | 10 | a0001c0001t0004g0271a0001c0001t0004g0284a0001c0001t0004g0285others(7): Show | 10 | HG01243.hp2 HG01975.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.237+30147A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904548 | ||||||
| chr12:79904615
|
T | A | 6 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012others(3): Show | 6 | HG01074.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+30080A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904615 | ||||||
| chr12:79904615
|
T | C | 30 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.237+30080A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904615 | ||||||
| chr12:79904720
|
G | A | 2 | a0001c0002t0002g0025a0001c0002t0002g0028 | 2 | HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.237+29975C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904720 | ||||||
| chr12:79904952
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+29743T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904952 | ||||||
| chr12:79904959
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0016g0227 | 2 | HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.237+29736A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79904959 | ||||||
| chr12:79905075
|
G | A | 183 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(180): Show | 184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.237+29620C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905075 | ||||||
| chr12:79905145
|
A | G | 1 | a0001c0002t0005g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.237+29550T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905145 | ||||||
| chr12:79905242
|
A | C | 1 | a0001c0001t0001g0188 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.237+29453T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905242 | ||||||
| chr12:79905326
|
G | A | 1 | a0001c0002t0005g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.237+29369C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905326 | ||||||
| chr12:79905339
|
G | GC | 37 | a0001c0001t0001g0198a0001c0001t0001g0212a0001c0001t0001g0213others(34): Show | 37 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.237+29355dupG | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905339 | ||||||
| chr12:79905339
|
G | GCC | 54 | a0001c0001t0001g0127a0001c0001t0001g0195a0001c0001t0001g0196others(51): Show | 54 | HG00408.hp1 HG00639.hp2 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.237+29354_237+2935 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905339 | ||||||
| chr12:79905339
|
G | GCCC | 91 | a0001c0001t0001g0130a0001c0001t0001g0194a0001c0001t0001g0204others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.237+29353_237+2935 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905339 | ||||||
| chr12:79905339
|
G | GCCCC | 17 | a0001c0001t0001g0188a0001c0001t0001g0211a0001c0001t0001g0243others(14): Show | 17 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.237+29352_237+2935 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905339 | ||||||
| chr12:79905342
|
C | T | 4 | a0001c0002t0005g0105a0001c0002t0005g0107a0001c0002t0005g0108others(1): Show | 4 | HG02809.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+29353G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905342 | ||||||
| chr12:79905387
|
T | C | 1 | a0001c0001t0004g0287 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.237+29308A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905387 | ||||||
| chr12:79905609
|
A | G | 1 | a0001c0001t0004g0291 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.237+29086T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905609 | ||||||
| chr12:79905688
|
C | T | 62 | a0001c0001t0001g0127a0001c0001t0001g0194a0001c0001t0001g0195others(59): Show | 62 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.237+29007G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79905688 | ||||||
| chr12:79906045
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+28650T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906045 | ||||||
| chr12:79906404
|
C | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.237+28291G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906404 | ||||||
| chr12:79906437
|
T | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+28258A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906437 | ||||||
| chr12:79906486
|
T | C | 3 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0013g0089 | 3 | HG02280.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.237+28209A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906486 | ||||||
| chr12:79906551
|
G | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0245 | 2 | HG02027.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237+28144C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906551 | ||||||
| chr12:79906598
|
C | CCTTT | 25 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(22): Show | 25 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.237+28096_237+2809 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906598 | ||||||
| chr12:79906599
|
A | C | 4 | a0001c0002t0005g0105a0001c0002t0005g0107a0001c0002t0005g0108others(1): Show | 4 | HG02809.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+28096T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906599 | ||||||
| chr12:79906601
|
T | G | 25 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(22): Show | 25 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.237+28094A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906601 | ||||||
| chr12:79906601
|
T | TTATG | 3 | a0001c0002t0002g0041a0001c0002t0009g0012a0001c0002t0009g0094 | 3 | HG02258.hp1 HG03041.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.237+28090_237+2809 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906601 | ||||||
| chr12:79906601
|
TTATG | T | 4 | a0001c0002t0005g0105a0001c0002t0005g0107a0001c0002t0005g0108others(1): Show | 4 | HG02809.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+28090_237+2809 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906601 | ||||||
| chr12:79906618
|
T | C | 2 | a0001c0001t0003g0171a0001c0001t0003g0172 | 2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.237+28077A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906618 | ||||||
| chr12:79906625
|
T | G | 6 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0001g0213others(3): Show | 6 | HG00423.hp2 NA18956.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.237+28070A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906625 | ||||||
| chr12:79906700
|
G | C | 1 | a0001c0001t0004g0305 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.237+27995C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906700 | ||||||
| chr12:79906727
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.237+27968A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906727 | ||||||
| chr12:79906855
|
C | T | 2 | a0001c0001t0003g0145a0001c0001t0003g0146 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.237+27840G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906855 | ||||||
| chr12:79906911
|
A | G | 3 | a0001c0001t0004g0274a0001c0001t0004g0275a0001c0001t0004g0288 | 3 | HG02040.hp1 NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.237+27784T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906911 | ||||||
| chr12:79906964
|
A | C | 1 | a0001c0001t0003g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.237+27731T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79906964 | ||||||
| chr12:79907014
|
C | T | 1 | a0001c0001t0004g0298 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.237+27681G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907014 | ||||||
| chr12:79907020
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.237+27675A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907020 | ||||||
| chr12:79907162
|
A | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+27533T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907162 | ||||||
| chr12:79907246
|
T | C | 125 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.237+27449A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907246 | ||||||
| chr12:79907248
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.237+27447A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907248 | ||||||
| chr12:79907456
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.237+27239T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907456 | ||||||
| chr12:79907476
|
G | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+27219C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907476 | ||||||
| chr12:79907493
|
G | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.237+27202C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907493 | ||||||
| chr12:79907497
|
G | A | 2 | a0001c0002t0002g0066a0001c0002t0002g0067 | 2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.237+27198C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907497 | ||||||
| chr12:79907618
|
T | G | 1 | a0001c0001t0001g0195 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.237+27077A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907618 | ||||||
| chr12:79907637
|
G | A | 39 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(36): Show | 39 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.237+27058C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79907637 | ||||||
| chr12:79908022
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+26673T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79908022 | ||||||
| chr12:79908170
|
T | G | 1 | a0001c0002t0006g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.237+26525A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79908170 | ||||||
| chr12:79908241
|
G | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+26454C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79908241 | ||||||
| chr12:79908349
|
A | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+26346T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79908349 | ||||||
| chr12:79908571
|
G | A | 123 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(120): Show | 123 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.237+26124C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79908571 | ||||||
| chr12:79908605
|
T | C | 1 | a0001c0002t0002g0068 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.237+26090A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79908605 | ||||||
| chr12:79908858
|
C | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+25837G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79908858 | ||||||
| chr12:79908924
|
T | C | 8 | a0001c0001t0001g0130a0001c0001t0003g0158a0001c0001t0003g0173others(5): Show | 8 | HG00408.hp2 HG00544.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+25771A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79908924 | ||||||
| chr12:79909676
|
C | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+25019G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79909676 | ||||||
| chr12:79909714
|
C | T | 3 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0013g0089 | 3 | HG02280.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.237+24981G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79909714 | ||||||
| chr12:79909727
|
TA | T | 8 | a0001c0001t0001g0254a0001c0002t0002g0043a0001c0002t0005g0002others(5): Show | 8 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.237+24967delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79909727 | ||||||
| chr12:79909727
|
TAA | T | 179 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(176): Show | 180 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.237+24966_237+2496 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79909727 | ||||||
| chr12:79909727
|
TAAA | T | 6 | a0001c0001t0001g0246a0001c0001t0003g0144a0001c0001t0003g0157others(3): Show | 6 | HG01256.hp1 HG01256.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+24965_237+2496 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79909727 | ||||||
| chr12:79909788
|
T | TTTG | 15 | a0001c0002t0006g0029a0001c0002t0006g0030a0001c0002t0006g0033others(12): Show | 15 | HG03710.hp2 HG03831.hp1 NA18906.hp2 others(12): Show |
intron_variant | MODIFIER | c.237+24904_237+2490 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79909788 | ||||||
| chr12:79909788
|
TTTGTTGT others(2): Show |
T | 4 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0177others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+24898_237+2490 others(13): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79909788 | ||||||
| chr12:79909818
|
G | A | 2 | a0001c0002t0006g0076a0001c0002t0006g0077 | 2 | NA18981.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.237+24877C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79909818 | ||||||
| chr12:79910040
|
T | C | 1 | a0001c0001t0004g0288 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.237+24655A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910040 | ||||||
| chr12:79910170
|
T | C | 1 | a0001c0001t0004g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.237+24525A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910170 | ||||||
| chr12:79910393
|
T | C | 3 | a0001c0002t0002g0038a0001c0002t0002g0039a0001c0002t0002g0040 | 3 | HG04199.hp2 NA19000.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.237+24302A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910393 | ||||||
| chr12:79910406
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+24289C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910406 | ||||||
| chr12:79910470
|
CAAAT | C | 253 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(250): Show | 254 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.237+24221_237+2422 others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910470 | ||||||
| chr12:79910548
|
T | TA | 213 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.237+24146dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910548 | ||||||
| chr12:79910548
|
T | TAA | 22 | a0001c0001t0001g0196a0001c0001t0001g0218a0001c0001t0001g0219others(19): Show | 22 | HG00639.hp2 HG01168.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.237+24145_237+2414 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910548 | ||||||
| chr12:79910654
|
G | A | 1 | a0001c0001t0003g0179 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.237+24041C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910654 | ||||||
| chr12:79910675
|
A | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+24020T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910675 | ||||||
| chr12:79910892
|
T | C | 34 | a0001c0001t0004g0001a0001c0001t0004g0268a0001c0001t0004g0269others(31): Show | 35 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.237+23803A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79910892 | ||||||
| chr12:79911011
|
A | C | 1 | a0001c0001t0004g0292 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.237+23684T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79911011 | ||||||
| chr12:79911030
|
C | A | 197 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(194): Show | 198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.237+23665G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79911030 | ||||||
| chr12:79911233
|
C | T | 2 | a0001c0002t0005g0106a0001c0002t0005g0111 | 2 | HG01192.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.237+23462G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79911233 | ||||||
| chr12:79911397
|
A | C | 1 | a0001c0001t0003g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.237+23298T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79911397 | ||||||
| chr12:79911439
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.237+23256A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79911439 | ||||||
| chr12:79911603
|
T | G | 2 | a0001c0001t0003g0180a0001c0001t0003g0181 | 2 | NA18939.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.237+23092A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79911603 | ||||||
| chr12:79911803
|
G | A | 1 | a0001c0002t0002g0070 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.237+22892C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79911803 | ||||||
| chr12:79912020
|
T | C | 1 | a0001c0002t0010g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.237+22675A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912020 | ||||||
| chr12:79912132
|
A | C | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.237+22563T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912132 | ||||||
| chr12:79912167
|
T | A | 1 | a0001c0001t0004g0290 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.237+22528A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912167 | ||||||
| chr12:79912226
|
A | T | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+22469T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912226 | ||||||
| chr12:79912612
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+22083A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912612 | ||||||
| chr12:79912623
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.237+22072C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912623 | ||||||
| chr12:79912689
|
A | AT | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+22005dupA | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912689 | ||||||
| chr12:79912692
|
T | A | 1 | a0001c0001t0016g0227 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.237+22003A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912692 | ||||||
| chr12:79912692
|
TA | T | 12 | a0001c0001t0001g0130a0001c0001t0001g0197a0001c0001t0001g0232others(9): Show | 12 | HG01099.hp1 HG01168.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.237+22002delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912692 | ||||||
| chr12:79912720
|
A | G | 4 | a0001c0002t0005g0101a0001c0002t0005g0102a0001c0002t0005g0103others(1): Show | 4 | HG01261.hp1 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+21975T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912720 | ||||||
| chr12:79912842
|
A | C | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+21853T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912842 | ||||||
| chr12:79912942
|
T | C | 51 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0300others(48): Show | 51 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.237+21753A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79912942 | ||||||
| chr12:79913053
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.237+21642C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913053 | ||||||
| chr12:79913141
|
A | G | 68 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0003g0006others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.237+21554T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913141 | ||||||
| chr12:79913198
|
C | T | 1 | a0001c0002t0009g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.237+21497G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913198 | ||||||
| chr12:79913202
|
T | C | 310 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(307): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.237+21493A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913202 | ||||||
| chr12:79913226
|
A | G | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+21469T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913226 | ||||||
| chr12:79913282
|
T | C | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+21413A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913282 | ||||||
| chr12:79913314
|
T | C | 1 | a0003c0008t0003g0131 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.237+21381A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913314 | ||||||
| chr12:79913387
|
G | A | 1 | a0001c0002t0006g0085 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.237+21308C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913387 | ||||||
| chr12:79913420
|
G | C | 1 | a0001c0001t0016g0227 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.237+21275C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913420 | ||||||
| chr12:79913609
|
G | A | 1 | a0001c0002t0002g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.237+21086C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913609 | ||||||
| chr12:79913642
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.237+21053A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913642 | ||||||
| chr12:79913697
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+20998G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913697 | ||||||
| chr12:79913715
|
C | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+20980G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913715 | ||||||
| chr12:79913951
|
T | C | 1 | a0001c0002t0006g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.237+20744A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913951 | ||||||
| chr12:79913976
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+20719A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79913976 | ||||||
| chr12:79914146
|
A | G | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.237+20549T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79914146 | ||||||
| chr12:79914190
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.237+20505C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79914190 | ||||||
| chr12:79914265
|
G | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+20430C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79914265 | ||||||
| chr12:79914274
|
T | G | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+20421A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79914274 | ||||||
| chr12:79914275
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.237+20420C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79914275 | ||||||
| chr12:79914859
|
T | A | 232 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(229): Show | 233 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.237+19836A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79914859 | ||||||
| chr12:79915114
|
T | C | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+19581A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915114 | ||||||
| chr12:79915315
|
T | C | 1 | a0001c0001t0004g0291 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.237+19380A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915315 | ||||||
| chr12:79915342
|
T | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(182): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.237+19353A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915342 | ||||||
| chr12:79915457
|
T | A | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+19238A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915457 | ||||||
| chr12:79915671
|
C | T | 2 | a0001c0002t0006g0076a0001c0002t0006g0077 | 2 | NA18981.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.237+19024G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915671 | ||||||
| chr12:79915785
|
T | C | 1 | a0001c0002t0005g0111 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.237+18910A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915785 | ||||||
| chr12:79915823
|
T | C | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.237+18872A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915823 | ||||||
| chr12:79915827
|
T | C | 2 | a0001c0002t0005g0002a0001c0002t0005g0003 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.237+18868A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915827 | ||||||
| chr12:79915835
|
T | C | 7 | a0001c0002t0006g0075a0001c0002t0006g0080a0001c0002t0006g0081others(4): Show | 7 | NA18939.hp1 NA18961.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+18860A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915835 | ||||||
| chr12:79915875
|
C | T | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0002t0002g0042 | 3 | HG01099.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.237+18820G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915875 | ||||||
| chr12:79915876
|
G | A | 2 | a0001c0001t0004g0270a0001c0001t0004g0292 | 2 | HG02523.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.237+18819C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79915876 | ||||||
| chr12:79916006
|
T | TAAAGATA others(315): Show |
1 | a0001c0001t0003g0183 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.237+18688_237+1868 others(326): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916006 | ||||||
| chr12:79916006
|
T | TAAAGATA others(315): Show |
42 | a0001c0001t0001g0130a0001c0001t0003g0006a0001c0001t0003g0129others(39): Show | 42 | HG00408.hp2 HG00741.hp2 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.237+18688_237+1868 others(326): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916006 | ||||||
| chr12:79916006
|
T | TAAAGATA others(316): Show |
8 | a0001c0001t0003g0184a0001c0001t0003g0186a0001c0001t0003g0187others(5): Show | 8 | HG00544.hp1 HG02572.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+18688_237+1868 others(327): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916006 | ||||||
| chr12:79916006
|
T | TAAAGATA others(317): Show |
1 | a0001c0001t0001g0188 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.237+18688_237+1868 others(328): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916006 | ||||||
| chr12:79916138
|
AAACAAAT others(12): Show |
A | 124 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0015others(121): Show | 124 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.237+18538_237+1855 others(23): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916138 | ||||||
| chr12:79916333
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.237+18362G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916333 | ||||||
| chr12:79916385
|
TA | T | 308 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(305): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.237+18309delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916385 | ||||||
| chr12:79916451
|
A | G | 10 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+18244T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916451 | ||||||
| chr12:79916493
|
T | C | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+18202A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916493 | ||||||
| chr12:79916548
|
T | TC | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+18146dupG | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916548 | ||||||
| chr12:79916578
|
A | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+18117T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916578 | ||||||
| chr12:79916674
|
T | C | 7 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0112others(4): Show | 7 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+18021A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916674 | ||||||
| chr12:79916772
|
A | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+17923T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916772 | ||||||
| chr12:79916784
|
T | C | 186 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(183): Show | 187 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.237+17911A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916784 | ||||||
| chr12:79916837
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0246 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.237+17858A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916837 | ||||||
| chr12:79916992
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.237+17703A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79916992 | ||||||
| chr12:79917185
|
T | C | 4 | a0001c0002t0002g0035a0001c0002t0002g0069a0001c0002t0002g0070others(1): Show | 4 | HG02074.hp1 NA18964.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+17510A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917185 | ||||||
| chr12:79917209
|
G | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.237+17486C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917209 | ||||||
| chr12:79917277
|
G | A | 30 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.237+17418C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917277 | ||||||
| chr12:79917337
|
T | C | 47 | a0001c0001t0004g0001a0001c0001t0004g0267a0001c0001t0004g0268others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.237+17358A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917337 | ||||||
| chr12:79917416
|
C | T | 1 | a0001c0006t0002g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.237+17279G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917416 | ||||||
| chr12:79917466
|
G | A | 1 | a0001c0001t0003g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.237+17229C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917466 | ||||||
| chr12:79917483
|
C | CA | 9 | a0001c0002t0002g0040a0001c0002t0002g0072a0001c0002t0002g0073others(6): Show | 9 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.237+17211dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917483 | ||||||
| chr12:79917483
|
CA | C | 15 | a0001c0001t0001g0233a0001c0001t0003g0189a0001c0001t0003g0190others(12): Show | 15 | HG02040.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.237+17211delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917483 | ||||||
| chr12:79917483
|
CAA | C | 174 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(171): Show | 175 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.237+17210_237+1721 others(6): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917483 | ||||||
| chr12:79917483
|
CAAA | C | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0003g0132others(3): Show | 6 | HG01943.hp2 HG01975.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.237+17209_237+1721 others(7): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917483 | ||||||
| chr12:79917506
|
G | A | 3 | a0001c0002t0005g0099a0002c0009t0005g0118a0004c0004t0005g0117 | 3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.237+17189C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917506 | ||||||
| chr12:79917647
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.237+17048A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917647 | ||||||
| chr12:79917649
|
C | CA | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+17045dupT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917649 | ||||||
| chr12:79917723
|
T | G | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.237+16972A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79917723 | ||||||
| chr12:79918639
|
A | G | 3 | a0001c0002t0002g0038a0001c0002t0002g0039a0001c0002t0002g0040 | 3 | HG04199.hp2 NA19000.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.237+16056T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79918639 | ||||||
| chr12:79918640
|
T | C | 47 | a0001c0001t0004g0001a0001c0001t0004g0267a0001c0001t0004g0268others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.237+16055A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79918640 | ||||||
| chr12:79918807
|
A | G | 12 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0300others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.237+15888T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79918807 | ||||||
| chr12:79918858
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.237+15837C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79918858 | ||||||
| chr12:79918884
|
G | C | 3 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0037 | 3 | HG02109.hp2 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.237+15811C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79918884 | ||||||
| chr12:79919085
|
C | A | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+15610G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79919085 | ||||||
| chr12:79919217
|
C | A | 6 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG00597.hp2 HG02027.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+15478G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79919217 | ||||||
| chr12:79919386
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+15309G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79919386 | ||||||
| chr12:79919422
|
G | A | 3 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296 | 3 | HG02165.hp2 NA18948.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.237+15273C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79919422 | ||||||
| chr12:79919502
|
C | G | 7 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0095others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+15193G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79919502 | ||||||
| chr12:79919760
|
T | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+14935A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79919760 | ||||||
| chr12:79920021
|
C | A | 12 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0300others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.237+14674G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79920021 | ||||||
| chr12:79920062
|
C | G | 1 | a0001c0002t0002g0074 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.237+14633G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79920062 | ||||||
| chr12:79920399
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+14296G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79920399 | ||||||
| chr12:79920850
|
T | C | 1 | a0001c0002t0005g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.237+13845A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79920850 | ||||||
| chr12:79921042
|
G | A | 1 | a0001c0002t0006g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.237+13653C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921042 | ||||||
| chr12:79921044
|
C | T | 29 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.237+13651G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921044 | ||||||
| chr12:79921060
|
C | T | 29 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.237+13635G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921060 | ||||||
| chr12:79921143
|
A | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | NA18981.hp2 NA18986.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+13552T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921143 | ||||||
| chr12:79921196
|
T | G | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+13499A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921196 | ||||||
| chr12:79921613
|
G | A | 1 | a0001c0002t0010g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.237+13082C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921613 | ||||||
| chr12:79921647
|
A | G | 1 | a0001c0001t0004g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.237+13048T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921647 | ||||||
| chr12:79921718
|
A | C | 3 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009 | 3 | HG02055.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.237+12977T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921718 | ||||||
| chr12:79921738
|
T | C | 1 | a0001c0001t0003g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.237+12957A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921738 | ||||||
| chr12:79921741
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.237+12954A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79921741 | ||||||
| chr12:79922197
|
G | A | 37 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(34): Show | 37 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.237+12498C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922197 | ||||||
| chr12:79922318
|
A | G | 70 | a0001c0001t0001g0127a0001c0001t0001g0194a0001c0001t0001g0195others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.237+12377T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922318 | ||||||
| chr12:79922367
|
T | C | 3 | a0001c0002t0005g0099a0002c0009t0005g0118a0004c0004t0005g0117 | 3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.237+12328A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922367 | ||||||
| chr12:79922372
|
C | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+12323G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922372 | ||||||
| chr12:79922750
|
C | T | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+11945G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922750 | ||||||
| chr12:79922788
|
A | T | 1 | a0001c0002t0002g0074 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.237+11907T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922788 | ||||||
| chr12:79922854
|
T | A | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG00639.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.237+11841A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922854 | ||||||
| chr12:79922859
|
T | TAAAAAGT others(320): Show |
1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+11835_237+1183 others(331): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922859 | ||||||
| chr12:79922897
|
G | A | 1 | a0001c0002t0005g0124 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.237+11798C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922897 | ||||||
| chr12:79922978
|
A | G | 197 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(194): Show | 198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.237+11717T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79922978 | ||||||
| chr12:79923143
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.237+11552C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923143 | ||||||
| chr12:79923211
|
T | A | 4 | a0001c0002t0006g0005a0001c0002t0006g0034a0001c0002t0006g0036others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+11484A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923211 | ||||||
| chr12:79923223
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02683.hp1 HG03017.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+11472C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923223 | ||||||
| chr12:79923342
|
A | C | 1 | a0001c0002t0005g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.237+11353T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923342 | ||||||
| chr12:79923406
|
C | T | 1 | a0001c0001t0004g0270 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.237+11289G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923406 | ||||||
| chr12:79923535
|
T | C | 4 | a0001c0002t0005g0119a0001c0002t0005g0120a0001c0002t0005g0121others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+11160A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923535 | ||||||
| chr12:79923555
|
C | T | 254 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(251): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.237+11140G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923555 | ||||||
| chr12:79923616
|
G | C | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | NA18969.hp2 NA18981.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.237+11079C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923616 | ||||||
| chr12:79923900
|
C | G | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+10795G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923900 | ||||||
| chr12:79923901
|
G | A | 1 | a0001c0001t0004g0306 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.237+10794C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923901 | ||||||
| chr12:79923976
|
G | A | 1 | a0001c0002t0009g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.237+10719C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923976 | ||||||
| chr12:79923979
|
G | A | 6 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG00597.hp2 HG02027.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+10716C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79923979 | ||||||
| chr12:79924401
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+10294A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79924401 | ||||||
| chr12:79924473
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+10222C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79924473 | ||||||
| chr12:79924783
|
A | C | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+9912T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79924783 | ||||||
| chr12:79924794
|
T | C | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+9901A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79924794 | ||||||
| chr12:79924912
|
T | C | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+9783A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79924912 | ||||||
| chr12:79925021
|
G | A | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+9674C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925021 | ||||||
| chr12:79925193
|
T | C | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+9502A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925193 | ||||||
| chr12:79925241
|
A | T | 1 | a0003c0008t0003g0131 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.237+9454T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925241 | ||||||
| chr12:79925261
|
C | CGT | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+9432_237+9433d others(4): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925261 | ||||||
| chr12:79925261
|
C | CGTGTGT | 4 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+9428_237+9433d others(8): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925261 | ||||||
| chr12:79925269
|
T | C | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.237+9426A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925269 | ||||||
| chr12:79925275
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+9420A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925275 | ||||||
| chr12:79925391
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.237+9304A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925391 | ||||||
| chr12:79925721
|
C | T | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+8974G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925721 | ||||||
| chr12:79925853
|
G | C | 189 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(186): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.237+8842C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925853 | ||||||
| chr12:79925864
|
A | G | 2 | a0001c0002t0006g0005a0001c0002t0006g0034 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.237+8831T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925864 | ||||||
| chr12:79925877
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+8818A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925877 | ||||||
| chr12:79925936
|
C | T | 4 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+8759G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925936 | ||||||
| chr12:79925937
|
T | C | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.237+8758A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79925937 | ||||||
| chr12:79926006
|
T | C | 1 | a0001c0001t0004g0307 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.237+8689A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926006 | ||||||
| chr12:79926124
|
A | C | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.237+8571T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926124 | ||||||
| chr12:79926216
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.237+8479G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926216 | ||||||
| chr12:79926225
|
G | A | 1 | a0001c0001t0004g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.237+8470C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926225 | ||||||
| chr12:79926471
|
G | A | 38 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(35): Show | 38 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.237+8224C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926471 | ||||||
| chr12:79926477
|
C | G | 1 | a0001c0002t0005g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.237+8218G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926477 | ||||||
| chr12:79926521
|
C | T | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.237+8174G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926521 | ||||||
| chr12:79926565
|
A | G | 1 | a0001c0002t0002g0035 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.237+8130T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926565 | ||||||
| chr12:79926681
|
T | A | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+8014A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926681 | ||||||
| chr12:79926744
|
GA | G | 234 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(231): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.237+7950delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926744 | ||||||
| chr12:79926775
|
G | A | 8 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0008g0090others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+7920C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926775 | ||||||
| chr12:79926791
|
T | C | 1 | a0001c0002t0002g0028 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.237+7904A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926791 | ||||||
| chr12:79926793
|
C | A | 15 | a0001c0002t0002g0074a0001c0002t0006g0029a0001c0002t0006g0030others(12): Show | 15 | HG03710.hp2 HG03831.hp1 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.237+7902G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79926793 | ||||||
| chr12:79927003
|
C | T | 188 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(185): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.237+7692G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927003 | ||||||
| chr12:79927015
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.237+7680C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927015 | ||||||
| chr12:79927032
|
GA | G | 188 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(185): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.237+7662delT | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927032 | ||||||
| chr12:79927085
|
C | T | 1 | a0001c0002t0006g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.237+7610G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927085 | ||||||
| chr12:79927205
|
A | G | 29 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.237+7490T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927205 | ||||||
| chr12:79927240
|
G | A | 141 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0194others(138): Show | 141 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.237+7455C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927240 | ||||||
| chr12:79927348
|
T | C | 3 | a0001c0002t0008g0087a0001c0002t0008g0088a0001c0002t0013g0089 | 3 | HG02280.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.237+7347A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927348 | ||||||
| chr12:79927516
|
C | G | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+7179G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927516 | ||||||
| chr12:79927564
|
C | A | 12 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(9): Show | 12 | HG00438.hp2 HG03834.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.237+7131G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927564 | ||||||
| chr12:79927619
|
C | A | 1 | a0001c0001t0001g0260 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.237+7076G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927619 | ||||||
| chr12:79927876
|
C | T | 3 | a0001c0002t0002g0031a0001c0002t0002g0032a0001c0002t0002g0126 | 3 | HG02129.hp1 HG02165.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.237+6819G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927876 | ||||||
| chr12:79927885
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.237+6810G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927885 | ||||||
| chr12:79927974
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.237+6721A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79927974 | ||||||
| chr12:79928074
|
A | T | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+6621T>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79928074 | ||||||
| chr12:79928246
|
T | C | 1 | a0001c0002t0008g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.237+6449A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79928246 | ||||||
| chr12:79928288
|
A | G | 37 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(34): Show | 37 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.237+6407T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79928288 | ||||||
| chr12:79928698
|
T | G | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+5997A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79928698 | ||||||
| chr12:79928801
|
C | T | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.237+5894G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79928801 | ||||||
| chr12:79928811
|
G | A | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+5884C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79928811 | ||||||
| chr12:79928923
|
G | A | 3 | a0001c0002t0005g0122a0001c0002t0005g0123a0001c0002t0005g0124 | 3 | HG02258.hp2 HG02572.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.237+5772C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79928923 | ||||||
| chr12:79929040
|
G | T | 1 | a0001c0002t0006g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.237+5655C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79929040 | ||||||
| chr12:79929182
|
G | T | 1 | a0001c0002t0006g0029 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.237+5513C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79929182 | ||||||
| chr12:79929191
|
T | C | 1 | a0001c0001t0004g0309 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.237+5504A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79929191 | ||||||
| chr12:79929197
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+5498A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79929197 | ||||||
| chr12:79929226
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+5469A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79929226 | ||||||
| chr12:79929741
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.237+4954G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79929741 | ||||||
| chr12:79930478
|
G | A | 3 | a0001c0002t0009g0092a0001c0002t0009g0093a0006c0007t0009g0091 | 3 | HG01074.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.237+4217C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79930478 | ||||||
| chr12:79930599
|
C | T | 3 | a0001c0002t0010g0007a0001c0002t0010g0008a0001c0002t0010g0009 | 3 | HG02055.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.237+4096G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79930599 | ||||||
| chr12:79930634
|
T | C | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+4061A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79930634 | ||||||
| chr12:79930733
|
T | C | 12 | a0001c0001t0004g0298a0001c0001t0004g0299a0001c0001t0004g0300others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.237+3962A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79930733 | ||||||
| chr12:79930759
|
C | A | 1 | a0001c0003t0015g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.237+3936G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79930759 | ||||||
| chr12:79931021
|
C | T | 69 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0003g0006others(66): Show | 69 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.237+3674G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931021 | ||||||
| chr12:79931024
|
G | C | 1 | a0001c0001t0003g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.237+3671C>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931024 | ||||||
| chr12:79931073
|
C | A | 296 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(293): Show | 297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.237+3622G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931073 | ||||||
| chr12:79931421
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.237+3274C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931421 | ||||||
| chr12:79931458
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.237+3237C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931458 | ||||||
| chr12:79931548
|
A | G | 188 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(185): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.237+3147T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931548 | ||||||
| chr12:79931649
|
A | C | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+3046T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931649 | ||||||
| chr12:79931820
|
C | T | 2 | a0001c0001t0003g0128a0001c0001t0003g0264 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.237+2875G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931820 | ||||||
| chr12:79931850
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+2845C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931850 | ||||||
| chr12:79931982
|
T | G | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+2713A>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79931982 | ||||||
| chr12:79932031
|
T | C | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+2664A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932031 | ||||||
| chr12:79932088
|
G | A | 190 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(187): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.237+2607C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932088 | ||||||
| chr12:79932138
|
T | C | 1 | a0001c0001t0020g0310 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.237+2557A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932138 | ||||||
| chr12:79932222
|
A | C | 1 | a0001c0002t0006g0014 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.237+2473T>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932222 | ||||||
| chr12:79932365
|
A | G | 2 | a0001c0001t0004g0268a0001c0001t0004g0269 | 2 | HG00408.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.237+2330T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932365 | ||||||
| chr12:79932423
|
A | G | 1 | a0001c0002t0002g0013 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.237+2272T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932423 | ||||||
| chr12:79932478
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+2217C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932478 | ||||||
| chr12:79932492
|
T | A | 233 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(230): Show | 234 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.237+2203A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932492 | ||||||
| chr12:79932505
|
T | C | 1 | a0001c0002t0008g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.237+2190A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932505 | ||||||
| chr12:79932518
|
G | A | 4 | a0001c0002t0008g0095a0001c0002t0008g0096a0001c0002t0008g0097others(1): Show | 4 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+2177C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932518 | ||||||
| chr12:79932689
|
A | G | 3 | a0001c0002t0009g0010a0001c0002t0009g0011a0001c0002t0009g0012 | 3 | HG02559.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+2006T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79932689 | ||||||
| chr12:79933035
|
T | C | 29 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0099others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.237+1660A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933035 | ||||||
| chr12:79933397
|
T | A | 1 | a0001c0002t0005g0125 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237+1298A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933397 | ||||||
| chr12:79933403
|
G | A | 1 | a0001c0002t0002g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.237+1292C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933403 | ||||||
| chr12:79933422
|
G | A | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+1273C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933422 | ||||||
| chr12:79933433
|
C | A | 45 | a0001c0001t0004g0001a0001c0001t0004g0268a0001c0001t0004g0269others(42): Show | 46 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.237+1262G>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933433 | ||||||
| chr12:79933498
|
T | C | 1 | a0001c0001t0003g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.237+1197A>G | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933498 | ||||||
| chr12:79933506
|
C | G | 47 | a0001c0001t0004g0001a0001c0001t0004g0267a0001c0001t0004g0268others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.237+1189G>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933506 | ||||||
| chr12:79933563
|
C | T | 189 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(186): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.237+1132G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933563 | ||||||
| chr12:79933821
|
G | T | 1 | a0001c0002t0006g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.237+874C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933821 | ||||||
| chr12:79933838
|
A | G | 1 | a0001c0002t0006g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.237+857T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933838 | ||||||
| chr12:79933864
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.237+831C>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79933864 | ||||||
| chr12:79934020
|
G | A | 138 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(135): Show | 138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.237+675C>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79934020 | ||||||
| chr12:79934021
|
GGCA | G | 138 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(135): Show | 138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.237+671_237+673del others(3): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79934021 | ||||||
| chr12:79934026
|
GCCCTT | G | 138 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0188others(135): Show | 138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.237+664_237+668del others(5): Show |
PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79934026 | ||||||
| chr12:79934197
|
T | A | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+498A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79934197 | ||||||
| chr12:79934331
|
A | G | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+364T>C | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79934331 | ||||||
| chr12:79934383
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.237+312G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79934383 | ||||||
| chr12:79934495
|
T | A | 1 | a0001c0002t0010g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+200A>T | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79934495 | ||||||
| chr12:79934546
|
C | T | 2 | a0001c0002t0005g0002a0001c0002t0005g0003 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.237+149G>A | PPP1R12A | ENSG00000058272.19 | transcript | ENST00000450142.7 | protein_coding | 1/24 | chr12 | 79934546 |