Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 220965 |
|---|---|
| ensemblid | ENSG00000148541.13 |
| hgncid | 19371 |
| symbol | FAM13C |
| name | family with sequence similarity 13 member C |
| refseq_nuc | NM_198215.4 |
| refseq_prot | NP_937858.2 |
| ensembl_nuc | ENST00000618804.5 |
| ensembl_prot | ENSP00000481854.1 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 59246133 |
| end | 59362549 |
| strand | - |
| ver | v1.2 |
| region | chr10:59246133-59362549 |
| region5000 | chr10:59241133-59367549 |
| regionname0 | FAM13C_chr10_59246133_59362549 |
| regionname5000 | FAM13C_chr10_59241133_59367549 |
| 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 | 585 | 189 | 74 | 29 | 60 | 2 | 22 | 48 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0002 | 0/0 | 585 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0003 | 0/0 | 585 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0004 | 0/0 | 585 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0005 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0006 | 0/0 | 585 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0007 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| 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 | 1758 | 184 | 70 | 29 | 59 | 2 | 22 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0002 | 0/0 | 1758 | 6 | 4 | 2 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0003 | 0/0 | 1758 | 4 | 2 | 2 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0004 | 0/0 | 1758 | 3 | 3 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0005 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0006 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0007 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0008 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0009 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| c0010 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| 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 | 1572 | 173 | 78 | 32 | 44 | 2 | 16 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| t0002 | 0/0 | 1572 | 22 | 1 | 0 | 15 | 0 | 6 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| t0003 | 1/0 | 1571 | 4 | 3 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| t0004 | 0/0 | 1572 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| t0005 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| t0006 | 0/0 | 1572 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| t0007 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| t0008 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| 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 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| 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 | 1758 | 184 | 70 | 29 | 59 | 2 | 22 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0004 | 0/0 | 1758 | 3 | 3 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0006 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0007 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0002c0002 | 0/0 | 1758 | 6 | 4 | 2 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0003c0003 | 0/0 | 1758 | 4 | 2 | 2 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0004c0005 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0005c0008 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0006c0009 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0007c0010 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3329 | 154 | 64 | 28 | 43 | 2 | 16 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0001t0002 | 0/0 | 3329 | 22 | 1 | 0 | 15 | 0 | 6 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0001t0003 | 1/0 | 3328 | 4 | 3 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0001t0004 | 0/0 | 3329 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0001t0005 | 0/0 | 3329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0001t0007 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0001t0008 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0004t0001 | 0/0 | 3329 | 3 | 3 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0006t0001 | 0/0 | 3329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0001c0007t0001 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0002c0002t0001 | 0/0 | 3329 | 5 | 4 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0002c0002t0006 | 0/0 | 3329 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0003c0003t0001 | 0/0 | 3329 | 4 | 2 | 2 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0004c0005t0001 | 0/0 | 3329 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0005c0008t0001 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0006c0009t0001 | 0/0 | 3329 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| a0007c0010t0001 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | copy fasta | chr10 | 59241133 | 59367549 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0003g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0003c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0003c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0004c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0004c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0005c0008t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0006c0009t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0007c0010t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | FIN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0195 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0193 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01261 | hp2 | a0006 | c0009 | t0001 | g0142 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02451 | hp1 | a0005 | c0008 | t0001 | g0160 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0048 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0185 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02886 | hp1 | a0007 | c0010 | t0001 | g0148 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0192 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0059 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03453 | hp1 | a0004 | c0005 | t0001 | g0027 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0194 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19043 | hp1 | a0004 | c0005 | t0001 | g0149 | AFR | LWK | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19057 | hp1 | a0001 | c0006 | t0001 | g0109 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ASW | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01123 | hp1 | a0002 | c0002 | t0006 | g0198 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | USA | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | USA | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0083 | REF | REF | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0140 | REF | REF | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59262463
|
C | G | 1 | a0003 | 4 | HG00639.hp1 HG01243.hp1 HG02976.hp1 others(1): Show |
missense_variant | MODERATE | c.1207G>C | p.Glu403Gln | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/14 | 1296/3328 | 1207/1758 | 403/585 | chr10 | 59262463 | ||
| chr10:59262543
|
G | A | 1 | a0005 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1127C>T | p.Pro376Leu | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/14 | 1216/3328 | 1127/1758 | 376/585 | chr10 | 59262543 | ||
| chr10:59268611
|
C | T | 1 | a0004 | 2 | HG03453.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.884G>A | p.Ser295Asn | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/14 | 973/3328 | 884/1758 | 295/585 | chr10 | 59268611 | ||
| chr10:59323992
|
G | A | 1 | a0002 | 6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
missense_variant | MODERATE | c.439C>T | p.Pro147Ser | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/14 | 528/3328 | 439/1758 | 147/585 | chr10 | 59323992 | ||
| chr10:59352401
|
G | A | 1 | a0006 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.193C>T | p.Pro65Ser | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/14 | 282/3328 | 193/1758 | 65/585 | chr10 | 59352401 | ||
| chr10:59352418
|
G | A | 1 | a0007 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.176C>T | p.Ala59Val | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/14 | 265/3328 | 176/1758 | 59/585 | chr10 | 59352418 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59262533
|
C | T | 1 | a0001c0007 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.1137G>A | p.Ala379Ala | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/14 | 1226/3328 | 1137/1758 | 379/585 | chr10 | 59262533 | ||
| chr10:59268688
|
C | T | 1 | a0001c0006 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.807G>A | p.Pro269Pro | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/14 | 896/3328 | 807/1758 | 269/585 | chr10 | 59268688 | ||
| chr10:59302840
|
C | T | 1 | a0001c0004 | 3 | HG01891.hp2 HG02145.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.468G>A | p.Ser156Ser | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/14 | 557/3328 | 468/1758 | 156/585 | chr10 | 59302840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59246501
|
C | T | 1 | a0001c0001t0008 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1113G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 1113 | chr10 | 59246501 | |||||
| chr10:59246650
|
G | A | 1 | a0001c0001t0002 | 22 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*964C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 964 | chr10 | 59246650 | |||||
| chr10:59246776
|
A | G | 1 | a0001c0001t0007 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*838T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 838 | chr10 | 59246776 | |||||
| chr10:59247009
|
C | T | 1 | a0002c0002t0006 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 605 | chr10 | 59247009 | |||||
| chr10:59247042
|
G | GA | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*571dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 571 | chr10 | 59247042 | |||||
| chr10:59247214
|
A | G | 1 | a0001c0001t0005 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 400 | chr10 | 59247214 | |||||
| chr10:59362549
|
C | T | 1 | a0001c0001t0004 | 1 | HG02300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-89G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/14 | 89 | chr10 | 59362549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59247774
|
A | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1635-37T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59247774 | ||||||
| chr10:59247832
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.1635-95C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59247832 | ||||||
| chr10:59248029
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1635-292G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248029 | ||||||
| chr10:59248085
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1635-348C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248085 | ||||||
| chr10:59248126
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1635-389T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248126 | ||||||
| chr10:59248289
|
C | T | 7 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0150others(4): Show | 7 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1635-552G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248289 | ||||||
| chr10:59248609
|
AAGGGGTA others(1): Show |
A | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1635-880_1635-873d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248609 | ||||||
| chr10:59249032
|
T | C | 7 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(4): Show | 7 | HG01123.hp1 HG01433.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1635-1295A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249032 | ||||||
| chr10:59249040
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0078 | 2 | NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1635-1303A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249040 | ||||||
| chr10:59249066
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1635-1329T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249066 | ||||||
| chr10:59249212
|
G | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1635-1475C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249212 | ||||||
| chr10:59249265
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0154 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1635-1528C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249265 | ||||||
| chr10:59249274
|
T | G | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1635-1537A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249274 | ||||||
| chr10:59249319
|
G | GCGTGAAC | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1635-1589_1635-158 others(11): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249319 | ||||||
| chr10:59249320
|
C | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1635-1583G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249320 | ||||||
| chr10:59249321
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1635-1584C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249321 | ||||||
| chr10:59249372
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1635-1635G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249372 | ||||||
| chr10:59249389
|
G | A | 9 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0202others(6): Show | 9 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635-1652C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249389 | ||||||
| chr10:59249408
|
G | GA | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 106 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1635-1672dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249408 | ||||||
| chr10:59249408
|
GA | G | 8 | a0001c0001t0001g0091a0001c0001t0001g0151a0001c0001t0001g0165others(5): Show | 8 | HG01433.hp2 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1635-1672delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249408 | ||||||
| chr10:59249408
|
GAA | G | 23 | a0001c0001t0001g0187a0001c0001t0002g0008a0001c0001t0002g0014others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1635-1673_1635-167 others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249408 | ||||||
| chr10:59249726
|
CTGTT | C | 29 | a0001c0001t0001g0091a0001c0001t0001g0165a0001c0001t0001g0186others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1634+1845_1634+184 others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249726 | ||||||
| chr10:59249864
|
T | C | 1 | a0001c0001t0001g0083 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1634+1711A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249864 | ||||||
| chr10:59249936
|
C | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1634+1639G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249936 | ||||||
| chr10:59250633
|
C | T | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1634+942G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250633 | ||||||
| chr10:59250637
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1634+938T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250637 | ||||||
| chr10:59250783
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1634+792C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250783 | ||||||
| chr10:59250874
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(43): Show | 47 | HG00639.hp2 HG01070.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.1634+701T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250874 | ||||||
| chr10:59250883
|
C | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634+692G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250883 | ||||||
| chr10:59251073
|
A | G | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1634+502T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251073 | ||||||
| chr10:59251115
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.1634+460C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251115 | ||||||
| chr10:59251314
|
T | C | 1 | a0001c0006t0001g0109 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1634+261A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251314 | ||||||
| chr10:59251336
|
G | A | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1634+239C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251336 | ||||||
| chr10:59251465
|
A | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1634+110T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251465 | ||||||
| chr10:59251565
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(40): Show | 44 | HG00639.hp2 HG01070.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1634+10G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251565 | ||||||
| chr10:59251566
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1634+9C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251566 | ||||||
| chr10:59251821
|
A | T | 1 | a0001c0001t0002g0014 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1533-145T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59251821 | ||||||
| chr10:59252014
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.1533-338G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59252014 | ||||||
| chr10:59252112
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1533-436T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59252112 | ||||||
| chr10:59252214
|
G | A | 11 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0202others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533-538C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59252214 | ||||||
| chr10:59252327
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1532+472C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59252327 | ||||||
| chr10:59253159
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1333-161G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253159 | ||||||
| chr10:59253457
|
C | T | 5 | a0001c0001t0001g0174a0001c0001t0001g0191a0002c0002t0001g0017others(2): Show | 5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-459G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253457 | ||||||
| chr10:59253688
|
AG | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0147 | 3 | NA18970.hp2 NA18988.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1332+659delC | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253688 | ||||||
| chr10:59253689
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(192): Show |
intron_variant | MODIFIER | c.1332+659C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253689 | ||||||
| chr10:59253791
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1332+557C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253791 | ||||||
| chr10:59254004
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0087 | 2 | NA18947.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1332+344G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59254004 | ||||||
| chr10:59254020
|
T | C | 5 | a0001c0001t0001g0174a0001c0001t0001g0191a0002c0002t0001g0017others(2): Show | 5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332+328A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59254020 | ||||||
| chr10:59254296
|
C | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1332+52G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59254296 | ||||||
| chr10:59254576
|
C | CATTT | 17 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(14): Show | 17 | HG01099.hp1 HG01099.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1237-137_1237-134d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254576 | ||||||
| chr10:59254576
|
CATTT | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 115 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(112): Show |
intron_variant | MODIFIER | c.1237-137_1237-134d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254576 | ||||||
| chr10:59254576
|
CATTTATT others(1): Show |
C | 20 | a0001c0001t0001g0033a0001c0001t0001g0061a0001c0001t0001g0165others(17): Show | 20 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1237-141_1237-134d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254576 | ||||||
| chr10:59254576
|
CATTTATT others(5): Show |
C | 23 | a0001c0001t0001g0091a0001c0001t0001g0183a0001c0001t0001g0184others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1237-145_1237-134d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254576 | ||||||
| chr10:59254650
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1237-207G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254650 | ||||||
| chr10:59254658
|
A | C | 4 | a0003c0003t0001g0192a0003c0003t0001g0193a0003c0003t0001g0194others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-215T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254658 | ||||||
| chr10:59254817
|
T | C | 7 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(4): Show | 7 | HG01123.hp1 HG01433.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1237-374A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254817 | ||||||
| chr10:59254857
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-414C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254857 | ||||||
| chr10:59254859
|
C | G | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1237-416G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254859 | ||||||
| chr10:59254883
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1237-440G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254883 | ||||||
| chr10:59255010
|
G | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0137 | 2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1237-567C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255010 | ||||||
| chr10:59255186
|
C | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0054others(8): Show | 11 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237-743G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255186 | ||||||
| chr10:59255212
|
T | C | 7 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(4): Show | 7 | HG01123.hp1 HG01433.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1237-769A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255212 | ||||||
| chr10:59255427
|
TTGTC | T | 9 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0202others(6): Show | 9 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1237-988_1237-985d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255427 | ||||||
| chr10:59255554
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0132a0001c0001t0001g0145 | 3 | NA18939.hp2 NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1237-1111A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255554 | ||||||
| chr10:59256256
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.1237-1813C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256256 | ||||||
| chr10:59256415
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-1972T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256415 | ||||||
| chr10:59256502
|
A | G | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1237-2059T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256502 | ||||||
| chr10:59256548
|
T | C | 12 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0200others(9): Show | 12 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1237-2105A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256548 | ||||||
| chr10:59256584
|
C | A | 1 | a0001c0001t0001g0133 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1237-2141G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256584 | ||||||
| chr10:59256873
|
T | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1237-2430A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256873 | ||||||
| chr10:59256884
|
A | G | 1 | a0006c0009t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1237-2441T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256884 | ||||||
| chr10:59256907
|
A | T | 6 | a0002c0002t0001g0037a0002c0002t0001g0095a0003c0003t0001g0192others(3): Show | 6 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237-2464T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256907 | ||||||
| chr10:59256992
|
A | G | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1237-2549T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256992 | ||||||
| chr10:59257018
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1237-2575G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257018 | ||||||
| chr10:59257079
|
T | C | 5 | a0001c0001t0001g0174a0001c0001t0001g0191a0002c0002t0001g0017others(2): Show | 5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1237-2636A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257079 | ||||||
| chr10:59257480
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1237-3037A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257480 | ||||||
| chr10:59257858
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1237-3415T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257858 | ||||||
| chr10:59257868
|
A | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1237-3425T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257868 | ||||||
| chr10:59258345
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1237-3902A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258345 | ||||||
| chr10:59258353
|
C | T | 1 | a0005c0008t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1237-3910G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258353 | ||||||
| chr10:59258367
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-3924G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258367 | ||||||
| chr10:59258490
|
T | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 108 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1236+3944A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258490 | ||||||
| chr10:59258631
|
G | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1236+3803C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258631 | ||||||
| chr10:59258726
|
G | A | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1236+3708C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258726 | ||||||
| chr10:59259058
|
T | A | 4 | a0001c0001t0001g0122a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG02451.hp2 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+3376A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59259058 | ||||||
| chr10:59259924
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(40): Show | 44 | HG00639.hp2 HG01070.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1236+2510C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59259924 | ||||||
| chr10:59260066
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1236+2368G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260066 | ||||||
| chr10:59260069
|
A | AT | 9 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0150others(6): Show | 9 | HG01070.hp1 HG01106.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1236+2364dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260069 | ||||||
| chr10:59260091
|
C | T | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0004c0005t0001g0027others(1): Show | 4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+2343G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260091 | ||||||
| chr10:59260112
|
A | G | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1236+2322T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260112 | ||||||
| chr10:59260150
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.1236+2284T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260150 | ||||||
| chr10:59260160
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1236+2274G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260160 | ||||||
| chr10:59260180
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1236+2254G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260180 | ||||||
| chr10:59260986
|
A | G | 1 | a0001c0007t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1236+1448T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260986 | ||||||
| chr10:59261201
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1236+1233A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261201 | ||||||
| chr10:59261396
|
T | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1236+1038A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261396 | ||||||
| chr10:59261518
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1236+916G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261518 | ||||||
| chr10:59261649
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1236+785T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261649 | ||||||
| chr10:59261805
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1236+629G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261805 | ||||||
| chr10:59261816
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1236+618G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261816 | ||||||
| chr10:59262280
|
G | A | 1 | a0001c0001t0005g0120 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1236+154C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59262280 | ||||||
| chr10:59262294
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1236+140C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59262294 | ||||||
| chr10:59262704
|
A | G | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1025-59T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59262704 | ||||||
| chr10:59263224
|
A | C | 11 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0054others(8): Show | 11 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1025-579T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263224 | ||||||
| chr10:59263335
|
T | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-690A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263335 | ||||||
| chr10:59263463
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.1024+622A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263463 | ||||||
| chr10:59263785
|
C | A | 1 | a0001c0001t0002g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1024+300G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263785 | ||||||
| chr10:59263892
|
A | G | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1024+193T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263892 | ||||||
| chr10:59263934
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1024+151C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263934 | ||||||
| chr10:59264201
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.943-35T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264201 | ||||||
| chr10:59264313
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.943-147C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264313 | ||||||
| chr10:59264598
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.943-432C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264598 | ||||||
| chr10:59264629
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.943-463G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264629 | ||||||
| chr10:59264695
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.943-529C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264695 | ||||||
| chr10:59264703
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.943-537G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264703 | ||||||
| chr10:59264758
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 131 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.943-592T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264758 | ||||||
| chr10:59264903
|
A | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.943-737T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264903 | ||||||
| chr10:59264929
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0022others(19): Show | 22 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.943-763C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264929 | ||||||
| chr10:59264986
|
C | A | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.943-820G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264986 | ||||||
| chr10:59265273
|
C | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.943-1107G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265273 | ||||||
| chr10:59265286
|
C | T | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.943-1120G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265286 | ||||||
| chr10:59265306
|
A | G | 7 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0187others(4): Show | 7 | HG00639.hp2 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.943-1140T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265306 | ||||||
| chr10:59265310
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0187a0001c0001t0001g0191others(3): Show | 6 | HG00639.hp2 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-1144T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265310 | ||||||
| chr10:59265311
|
A | AGGGG | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0044others(5): Show | 8 | HG01891.hp1 HG02135.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.943-1149_943-1146d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265311 | ||||||
| chr10:59265311
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0187a0001c0001t0001g0191others(3): Show | 6 | HG00639.hp2 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-1145T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265311 | ||||||
| chr10:59265315
|
GT | G | 4 | a0001c0001t0001g0091a0001c0001t0002g0063a0001c0001t0002g0075others(1): Show | 4 | HG02698.hp2 HG03579.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.943-1150delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265315 | ||||||
| chr10:59265315
|
GTT | G | 19 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0020others(16): Show | 19 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.943-1151_943-1150d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265315 | ||||||
| chr10:59265316
|
T | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(62): Show | 66 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.943-1150A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265316 | ||||||
| chr10:59265317
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.943-1151A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265317 | ||||||
| chr10:59265317
|
T | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(64): Show | 68 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.943-1151A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265317 | ||||||
| chr10:59265318
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943-1152A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265318 | ||||||
| chr10:59265318
|
T | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(67): Show | 71 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.943-1152A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265318 | ||||||
| chr10:59265319
|
T | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(88): Show | 92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.943-1153A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265319 | ||||||
| chr10:59265322
|
C | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(68): Show | 71 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.943-1156G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265322 | ||||||
| chr10:59265323
|
G | T | 3 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0125 | 3 | HG02698.hp2 NA18956.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.943-1157C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265323 | ||||||
| chr10:59265324
|
G | T | 19 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0020others(16): Show | 19 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.943-1158C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265324 | ||||||
| chr10:59265325
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.943-1159C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265325 | ||||||
| chr10:59265327
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0110a0001c0001t0001g0133others(1): Show | 4 | HG02698.hp1 NA18994.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.943-1161C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265327 | ||||||
| chr10:59265327
|
G | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(13): Show | 17 | HG01106.hp1 HG01891.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.943-1161C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265327 | ||||||
| chr10:59265327
|
G | GAGC | 5 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.943-1162_943-1161i others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265327 | ||||||
| chr10:59265331
|
G | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0051others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.943-1165C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265331 | ||||||
| chr10:59265332
|
G | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(36): Show | 40 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.943-1166C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265332 | ||||||
| chr10:59265332
|
G | GCGGGGC | 8 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0112others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-1167_943-1166i others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265332 | ||||||
| chr10:59265335
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(84): Show | 88 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.943-1169C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GCGGA | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0051others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GGCGGGGC others(3): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0143 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.943-1170_943-1169i others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GGGGGGA | 14 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(11): Show | 14 | HG00609.hp2 HG01081.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GGGGGGGA | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GGGGGGGG others(2): Show |
17 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0038others(14): Show | 17 | HG00597.hp1 HG00609.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(11): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GGGGGGGG others(3): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0033others(2): Show | 5 | HG01070.hp2 HG02622.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GGGGGGGG others(4): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0030 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.943-1170_943-1169i others(13): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GGGGGGGG others(5): Show |
1 | a0001c0001t0001g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.943-1170_943-1169i others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265335
|
G | GGGGGGGG others(6): Show |
1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.943-1170_943-1169i others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | ||||||
| chr10:59265380
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.943-1214G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265380 | ||||||
| chr10:59265398
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(65): Show | 69 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.943-1232C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265398 | ||||||
| chr10:59265459
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.943-1293A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265459 | ||||||
| chr10:59265632
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0096 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.943-1466T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265632 | ||||||
| chr10:59265775
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.943-1609A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265775 | ||||||
| chr10:59265796
|
G | C | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.943-1630C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265796 | ||||||
| chr10:59266060
|
A | T | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.943-1894T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266060 | ||||||
| chr10:59266182
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0172 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.943-2016A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266182 | ||||||
| chr10:59266218
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112 | 3 | HG03704.hp1 HG03927.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.943-2052C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266218 | ||||||
| chr10:59266221
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.943-2055C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266221 | ||||||
| chr10:59266407
|
A | G | 24 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0020others(21): Show | 24 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.942+2146T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266407 | ||||||
| chr10:59266490
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(88): Show | 92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.942+2063G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266490 | ||||||
| chr10:59266538
|
A | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(92): Show | 96 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.942+2015T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266538 | ||||||
| chr10:59266570
|
A | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(88): Show | 92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.942+1983T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266570 | ||||||
| chr10:59266886
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.942+1667T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266886 | ||||||
| chr10:59266901
|
A | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0153a0001c0001t0001g0201 | 3 | HG01891.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.942+1652T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266901 | ||||||
| chr10:59267033
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.942+1520A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267033 | ||||||
| chr10:59267145
|
G | T | 1 | a0001c0001t0002g0064 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.942+1408C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267145 | ||||||
| chr10:59267199
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0078 | 2 | NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.942+1354C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267199 | ||||||
| chr10:59267351
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.942+1202G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267351 | ||||||
| chr10:59267366
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.942+1187G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267366 | ||||||
| chr10:59267494
|
C | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(43): Show | 47 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.942+1059G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267494 | ||||||
| chr10:59267652
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.942+901C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267652 | ||||||
| chr10:59267801
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.942+752G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267801 | ||||||
| chr10:59268008
|
C | T | 1 | a0001c0001t0005g0120 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.942+545G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268008 | ||||||
| chr10:59268226
|
A | AAAG | 4 | a0001c0001t0001g0021a0001c0001t0001g0096a0004c0005t0001g0027others(1): Show | 4 | HG03453.hp1 HG03831.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+324_942+326dup others(3): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268226 | ||||||
| chr10:59268226
|
AAAGAAG | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(87): Show | 91 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.942+321_942+326del others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268226 | ||||||
| chr10:59268294
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0146 | 2 | NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.942+259T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268294 | ||||||
| chr10:59268430
|
T | G | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.942+123A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268430 | ||||||
| chr10:59268466
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0147 | 2 | NA18970.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.942+87C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268466 | ||||||
| chr10:59268518
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.942+35G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268518 | ||||||
| chr10:59268717
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(65): Show | 69 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.804-26C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59268717 | ||||||
| chr10:59269109
|
G | A | 9 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0202others(6): Show | 9 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-418C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269109 | ||||||
| chr10:59269417
|
T | TACACAC | 5 | a0001c0001t0001g0054a0001c0001t0001g0150a0001c0001t0001g0153others(2): Show | 5 | HG01106.hp1 HG01891.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+476_803+481dup others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | ||||||
| chr10:59269417
|
T | TACACACA others(1): Show |
17 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0067others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+474_803+481dup others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | ||||||
| chr10:59269417
|
T | TACACACA others(3): Show |
21 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0047others(18): Show | 21 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.803+472_803+481dup others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | ||||||
| chr10:59269417
|
T | TACACACA others(5): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0046others(9): Show | 13 | HG02486.hp2 HG02723.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.803+470_803+481dup others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | ||||||
| chr10:59269417
|
T | TACACACA others(7): Show |
12 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0089others(9): Show | 12 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+468_803+481dup others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | ||||||
| chr10:59269417
|
T | TACACACA others(11): Show |
1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.803+464_803+481dup others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | ||||||
| chr10:59269417
|
TAC | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.803+480_803+481del others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | ||||||
| chr10:59269417
|
TACAC | T | 3 | a0001c0001t0004g0128a0004c0005t0001g0027a0004c0005t0001g0149 | 3 | HG02300.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.803+478_803+481del others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | ||||||
| chr10:59269445
|
C | A | 7 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0065others(4): Show | 7 | NA18950.hp2 NA18956.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+454G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269445 | ||||||
| chr10:59269591
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.803+308C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269591 | ||||||
| chr10:59269616
|
T | C | 26 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0008others(23): Show | 26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.803+283A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269616 | ||||||
| chr10:59269725
|
G | GCAATGGC others(2): Show |
22 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0020others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.803+165_803+173dup others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269725 | ||||||
| chr10:59269778
|
G | A | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0004c0005t0001g0027others(1): Show | 4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+121C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269778 | ||||||
| chr10:59269814
|
C | T | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0004c0005t0001g0027others(1): Show | 4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+85G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269814 | ||||||
| chr10:59270217
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.593-108C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270217 | ||||||
| chr10:59270405
|
A | G | 26 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0008others(23): Show | 26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.593-296T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270405 | ||||||
| chr10:59270471
|
C | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.593-362G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270471 | ||||||
| chr10:59270519
|
GA | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(62): Show | 66 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.593-411delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270519 | ||||||
| chr10:59270643
|
T | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(88): Show | 92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.593-534A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270643 | ||||||
| chr10:59270666
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.593-557A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270666 | ||||||
| chr10:59270704
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.593-595A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270704 | ||||||
| chr10:59270816
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.593-707A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270816 | ||||||
| chr10:59270890
|
C | T | 6 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0150others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-781G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270890 | ||||||
| chr10:59270953
|
C | A | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0004c0005t0001g0027others(1): Show | 4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-844G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270953 | ||||||
| chr10:59270982
|
A | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(88): Show | 92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.593-873T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270982 | ||||||
| chr10:59271006
|
C | A | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-897G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271006 | ||||||
| chr10:59271112
|
G | C | 1 | a0001c0007t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.593-1003C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271112 | ||||||
| chr10:59271328
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.593-1219A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271328 | ||||||
| chr10:59271536
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.593-1427C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271536 | ||||||
| chr10:59271873
|
T | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(86): Show | 90 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.593-1764A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271873 | ||||||
| chr10:59271949
|
G | A | 1 | a0006c0009t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.593-1840C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271949 | ||||||
| chr10:59272023
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.593-1914A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272023 | ||||||
| chr10:59272458
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.593-2349T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272458 | ||||||
| chr10:59272494
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.593-2385G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272494 | ||||||
| chr10:59272506
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(89): Show | 93 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.593-2397C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272506 | ||||||
| chr10:59272515
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.593-2406A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272515 | ||||||
| chr10:59272659
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.593-2550C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272659 | ||||||
| chr10:59272747
|
C | T | 5 | a0001c0001t0001g0174a0001c0001t0001g0191a0002c0002t0001g0017others(2): Show | 5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-2638G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272747 | ||||||
| chr10:59272791
|
T | C | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0004c0005t0001g0027others(1): Show | 4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-2682A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272791 | ||||||
| chr10:59272865
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0141a0001c0001t0001g0143others(6): Show | 9 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593-2756C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272865 | ||||||
| chr10:59273074
|
G | A | 22 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0020others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.593-2965C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273074 | ||||||
| chr10:59273134
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-3025G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273134 | ||||||
| chr10:59273192
|
T | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(92): Show | 96 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.593-3083A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273192 | ||||||
| chr10:59273355
|
A | C | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.593-3246T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273355 | ||||||
| chr10:59273366
|
T | C | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.593-3257A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273366 | ||||||
| chr10:59273861
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.593-3752A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273861 | ||||||
| chr10:59274218
|
C | CATCTG | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(92): Show | 96 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.593-4110_593-4109i others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274218 | ||||||
| chr10:59274259
|
G | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.593-4150C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274259 | ||||||
| chr10:59274393
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.593-4284G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274393 | ||||||
| chr10:59274443
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.593-4334T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274443 | ||||||
| chr10:59274612
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0129 | 2 | HG01168.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.593-4503A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274612 | ||||||
| chr10:59274645
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.593-4536G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274645 | ||||||
| chr10:59274702
|
T | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(89): Show | 93 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.593-4593A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274702 | ||||||
| chr10:59275093
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.593-4984C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275093 | ||||||
| chr10:59275148
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.593-5039A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275148 | ||||||
| chr10:59275384
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.593-5275G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275384 | ||||||
| chr10:59275749
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00735.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.593-5640C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275749 | ||||||
| chr10:59275810
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(87): Show | 91 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.593-5701G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275810 | ||||||
| chr10:59276229
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.593-6120C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276229 | ||||||
| chr10:59276271
|
T | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0117 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.593-6162A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276271 | ||||||
| chr10:59276423
|
CA | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0013 | 2 | HG00609.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.593-6315delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276423 | ||||||
| chr10:59276453
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(89): Show | 93 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.593-6344C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276453 | ||||||
| chr10:59276544
|
G | C | 1 | a0001c0001t0002g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.593-6435C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276544 | ||||||
| chr10:59276635
|
G | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(9): Show | 12 | HG00673.hp2 HG01099.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.593-6526C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276635 | ||||||
| chr10:59276679
|
G | T | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 106 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.593-6570C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276679 | ||||||
| chr10:59276802
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.592+6561C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276802 | ||||||
| chr10:59276911
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.592+6452A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276911 | ||||||
| chr10:59276969
|
G | A | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+6394C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276969 | ||||||
| chr10:59277094
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.592+6269C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277094 | ||||||
| chr10:59277224
|
C | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+6139G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277224 | ||||||
| chr10:59277312
|
T | A | 1 | a0006c0009t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.592+6051A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277312 | ||||||
| chr10:59277613
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.592+5750C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277613 | ||||||
| chr10:59277735
|
T | C | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG02055.hp2 HG02451.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+5628A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277735 | ||||||
| chr10:59277895
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.592+5468G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277895 | ||||||
| chr10:59278462
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.592+4901C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278462 | ||||||
| chr10:59278506
|
C | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.592+4857G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278506 | ||||||
| chr10:59278656
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(23): Show | 27 | HG01884.hp1 HG01891.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.592+4707G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278656 | ||||||
| chr10:59278833
|
T | TAC | 4 | a0001c0001t0001g0019a0001c0001t0001g0169a0001c0001t0001g0188others(1): Show | 4 | HG00323.hp2 HG01070.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+4528_592+4529d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278833 | ||||||
| chr10:59278833
|
TAC | T | 14 | a0001c0001t0001g0151a0001c0001t0001g0178a0001c0001t0001g0200others(11): Show | 14 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.592+4528_592+4529d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278833 | ||||||
| chr10:59278833
|
TACAC | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(73): Show | 77 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.592+4526_592+4529d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278833 | ||||||
| chr10:59278862
|
T | C | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.592+4501A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278862 | ||||||
| chr10:59278957
|
G | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0050others(7): Show | 10 | HG02004.hp2 HG02698.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.592+4406C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278957 | ||||||
| chr10:59278979
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.592+4384A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278979 | ||||||
| chr10:59279091
|
C | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.592+4272G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279091 | ||||||
| chr10:59279183
|
C | T | 13 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0202others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.592+4180G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279183 | ||||||
| chr10:59279395
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.592+3968A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279395 | ||||||
| chr10:59279483
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.592+3880T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279483 | ||||||
| chr10:59279713
|
A | C | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+3650T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279713 | ||||||
| chr10:59279866
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0032others(1): Show | 4 | HG02622.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+3497A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279866 | ||||||
| chr10:59280166
|
C | A | 1 | a0001c0004t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.592+3197G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280166 | ||||||
| chr10:59280811
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.592+2552G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280811 | ||||||
| chr10:59280967
|
C | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+2396G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280967 | ||||||
| chr10:59280972
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.592+2391C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280972 | ||||||
| chr10:59280982
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(77): Show | 81 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.592+2381C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280982 | ||||||
| chr10:59281003
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.592+2360C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281003 | ||||||
| chr10:59281387
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1976C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281387 | ||||||
| chr10:59281422
|
C | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(24): Show | 28 | HG01884.hp1 HG01891.hp2 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.592+1941G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281422 | ||||||
| chr10:59281572
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1791A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281572 | ||||||
| chr10:59281854
|
A | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(81): Show | 85 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.592+1509T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281854 | ||||||
| chr10:59281951
|
G | T | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.592+1412C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281951 | ||||||
| chr10:59281962
|
T | G | 1 | a0001c0001t0002g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.592+1401A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281962 | ||||||
| chr10:59282245
|
C | A | 11 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0202others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.592+1118G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282245 | ||||||
| chr10:59282343
|
T | C | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0004c0005t0001g0027others(1): Show | 4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+1020A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282343 | ||||||
| chr10:59282474
|
T | G | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.592+889A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282474 | ||||||
| chr10:59282560
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+803T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282560 | ||||||
| chr10:59282764
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.592+599G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282764 | ||||||
| chr10:59282832
|
GA | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(80): Show | 84 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.592+530delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282832 | ||||||
| chr10:59282921
|
G | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(73): Show | 77 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.592+442C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282921 | ||||||
| chr10:59283156
|
C | A | 5 | a0001c0001t0001g0174a0001c0001t0001g0191a0002c0002t0001g0017others(2): Show | 5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+207G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59283156 | ||||||
| chr10:59283158
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.592+205C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59283158 | ||||||
| chr10:59283222
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592+141C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59283222 | ||||||
| chr10:59283291
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(45): Show | 49 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.592+72C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59283291 | ||||||
| chr10:59283484
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0136others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-37C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59283484 | ||||||
| chr10:59283678
|
C | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-231G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59283678 | ||||||
| chr10:59283691
|
G | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.508-244C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59283691 | ||||||
| chr10:59283826
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0164 | 3 | HG02572.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.508-379A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59283826 | ||||||
| chr10:59284031
|
A | ATG | 2 | a0001c0001t0001g0115a0001c0001t0001g0187 | 2 | HG00597.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.508-586_508-585dup others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | ||||||
| chr10:59284031
|
A | ATGTGTG | 26 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(23): Show | 26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.508-590_508-585dup others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | ||||||
| chr10:59284031
|
A | ATGTGTGT others(1): Show |
35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(32): Show | 36 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.508-592_508-585dup others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | ||||||
| chr10:59284031
|
A | ATGTGTGT others(3): Show |
7 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0091others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-594_508-585dup others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | ||||||
| chr10:59284031
|
A | ATGTGTGT others(5): Show |
5 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-596_508-585dup others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | ||||||
| chr10:59284031
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.508-584T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | ||||||
| chr10:59284031
|
ATGTG | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0141a0001c0001t0001g0143others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-588_508-585del others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | ||||||
| chr10:59284154
|
C | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-707G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284154 | ||||||
| chr10:59284276
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.508-829A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284276 | ||||||
| chr10:59284421
|
C | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-974G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284421 | ||||||
| chr10:59284423
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(81): Show | 85 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.508-976C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284423 | ||||||
| chr10:59284741
|
C | CCA | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(81): Show | 85 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.508-1296_508-1295d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284741 | ||||||
| chr10:59284816
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.508-1369T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284816 | ||||||
| chr10:59284839
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(91): Show | 95 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.508-1392A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284839 | ||||||
| chr10:59285105
|
C | A | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-1658G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285105 | ||||||
| chr10:59285311
|
G | C | 1 | a0002c0002t0001g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.508-1864C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285311 | ||||||
| chr10:59285398
|
C | CAG | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(91): Show | 95 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.508-1952_508-1951i others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285398 | ||||||
| chr10:59285742
|
G | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-2295C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285742 | ||||||
| chr10:59285804
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.508-2357G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285804 | ||||||
| chr10:59285885
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-2438A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285885 | ||||||
| chr10:59285961
|
C | CTG | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(91): Show | 95 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.508-2516_508-2515d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285961 | ||||||
| chr10:59286026
|
C | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-2579G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286026 | ||||||
| chr10:59286091
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.508-2644C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286091 | ||||||
| chr10:59286289
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.508-2842G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286289 | ||||||
| chr10:59286470
|
G | A | 9 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0202others(6): Show | 9 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-3023C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286470 | ||||||
| chr10:59286516
|
A | AAT | 4 | a0001c0001t0001g0174a0001c0001t0001g0191a0002c0002t0001g0017others(1): Show | 4 | HG00639.hp2 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-3071_508-3070d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATAT | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.508-3073_508-3070d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATAT | 39 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(36): Show | 40 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.508-3075_508-3070d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(1): Show |
11 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0101others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.508-3077_508-3070d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(3): Show |
1 | a0001c0007t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.508-3079_508-3070d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(5): Show |
5 | a0001c0001t0001g0002a0001c0001t0001g0112a0001c0001t0001g0143others(2): Show | 5 | HG02572.hp2 HG02886.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-3081_508-3070d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(7): Show |
3 | a0001c0001t0001g0051a0001c0001t0001g0196a0001c0001t0002g0135 | 3 | HG02257.hp2 HG03471.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.508-3083_508-3070d others(16): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(9): Show |
3 | a0001c0001t0001g0025a0001c0001t0001g0108a0001c0004t0001g0026 | 3 | HG00735.hp2 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.508-3085_508-3070d others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(11): Show |
4 | a0001c0001t0001g0070a0001c0001t0001g0107a0001c0001t0001g0153others(1): Show | 4 | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-3087_508-3070d others(20): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(13): Show |
3 | a0001c0001t0001g0054a0001c0001t0001g0091a0001c0001t0001g0151 | 3 | HG01433.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.508-3089_508-3070d others(22): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(17): Show |
4 | a0001c0001t0001g0045a0001c0001t0001g0067a0001c0001t0001g0172others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-3093_508-3070d others(26): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(21): Show |
1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.508-3070_508-3069i others(30): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(31): Show |
1 | a0001c0001t0002g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.508-3070_508-3069i others(40): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(23): Show |
2 | a0001c0001t0001g0089a0001c0001t0002g0014 | 2 | NA18959.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(32): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(25): Show |
2 | a0001c0001t0002g0071a0001c0001t0002g0170 | 2 | HG00673.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(34): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(27): Show |
1 | a0001c0001t0002g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.508-3070_508-3069i others(36): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(29): Show |
2 | a0001c0001t0002g0064a0001c0001t0002g0077 | 2 | HG00558.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(38): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(31): Show |
2 | a0001c0001t0002g0074a0001c0001t0002g0119 | 2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(40): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(33): Show |
5 | a0001c0001t0002g0008a0001c0001t0002g0068a0001c0001t0002g0075others(2): Show | 5 | HG02698.hp2 HG03540.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-3070_508-3069i others(42): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(37): Show |
2 | a0001c0001t0002g0063a0001c0001t0002g0130 | 2 | NA18994.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(46): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(41): Show |
2 | a0001c0001t0002g0062a0001c0001t0002g0065 | 2 | NA18988.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(50): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | AATATATA others(45): Show |
1 | a0001c0001t0002g0125 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.508-3070_508-3069i others(54): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | ATATATAT | 2 | a0001c0001t0001g0076a0001c0001t0001g0123 | 2 | HG02132.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.508-3070_508-3069i others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
A | ATATATAT others(24): Show |
1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.508-3070_508-3069i others(33): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
AAT | A | 6 | a0001c0001t0001g0187a0003c0003t0001g0192a0003c0003t0001g0193others(3): Show | 6 | HG00639.hp1 HG01243.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-3071_508-3070d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
AATAT | A | 14 | a0001c0001t0001g0165a0001c0001t0001g0178a0001c0001t0001g0180others(11): Show | 14 | HG01167.hp1 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.508-3073_508-3070d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
AATATAT | A | 3 | a0001c0001t0007g0185a0004c0005t0001g0027a0004c0005t0001g0149 | 3 | HG02647.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3075_508-3070d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286516
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0002g0081 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.508-3079_508-3070d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | ||||||
| chr10:59286786
|
C | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(71): Show | 75 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.508-3339G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286786 | ||||||
| chr10:59286791
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-3344A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286791 | ||||||
| chr10:59286804
|
C | T | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508-3357G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286804 | ||||||
| chr10:59286890
|
C | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3443G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286890 | ||||||
| chr10:59286905
|
G | C | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3458C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286905 | ||||||
| chr10:59286972
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.508-3525A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286972 | ||||||
| chr10:59286988
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.508-3541G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286988 | ||||||
| chr10:59287010
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0032others(2): Show | 5 | HG02622.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-3563C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287010 | ||||||
| chr10:59287021
|
G | A | 10 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0054others(7): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-3574C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287021 | ||||||
| chr10:59287033
|
C | CA | 18 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0164others(15): Show | 18 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.508-3587dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287033 | ||||||
| chr10:59287033
|
CA | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(38): Show | 42 | HG00323.hp1 HG00639.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.508-3587delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287033 | ||||||
| chr10:59287105
|
G | A | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508-3658C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287105 | ||||||
| chr10:59287200
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.508-3753C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287200 | ||||||
| chr10:59287284
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.508-3837A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287284 | ||||||
| chr10:59287295
|
C | A | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3848G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287295 | ||||||
| chr10:59287331
|
T | A | 12 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0200others(9): Show | 12 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-3884A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287331 | ||||||
| chr10:59287336
|
CAA | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0025others(21): Show | 24 | HG00597.hp1 HG01243.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.508-3891_508-3890d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | ||||||
| chr10:59287336
|
CAAA | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(68): Show | 71 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.508-3892_508-3890d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | ||||||
| chr10:59287336
|
CAAAA | C | 16 | a0001c0001t0001g0024a0001c0001t0001g0050a0001c0001t0001g0055others(13): Show | 16 | HG00558.hp1 HG01070.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.508-3893_508-3890d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | ||||||
| chr10:59287336
|
CAAAAA | C | 17 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0054others(14): Show | 17 | HG01106.hp1 HG01123.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.508-3894_508-3890d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | ||||||
| chr10:59287336
|
CAAAAAA | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(42): Show | 46 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.508-3895_508-3890d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | ||||||
| chr10:59287336
|
CAAAAAAA | C | 16 | a0001c0001t0001g0051a0001c0001t0001g0143a0001c0001t0001g0155others(13): Show | 16 | HG02109.hp1 HG02572.hp2 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.508-3896_508-3890d others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | ||||||
| chr10:59287367
|
G | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0136others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-3920C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287367 | ||||||
| chr10:59287579
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.508-4132C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287579 | ||||||
| chr10:59287740
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.508-4293T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287740 | ||||||
| chr10:59287757
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.508-4310A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287757 | ||||||
| chr10:59287808
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.508-4361A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287808 | ||||||
| chr10:59288218
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508-4771C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288218 | ||||||
| chr10:59288337
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.508-4890A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288337 | ||||||
| chr10:59288363
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508-4916G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288363 | ||||||
| chr10:59288483
|
A | AAAG | 11 | a0001c0001t0001g0091a0001c0001t0001g0122a0001c0001t0001g0165others(8): Show | 11 | HG02055.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.508-5039_508-5037d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288483 | ||||||
| chr10:59288483
|
AAAG | A | 23 | a0001c0001t0001g0046a0001c0001t0002g0008a0001c0001t0002g0014others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.508-5039_508-5037d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288483 | ||||||
| chr10:59289076
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.508-5629G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289076 | ||||||
| chr10:59289165
|
C | T | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508-5718G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289165 | ||||||
| chr10:59289275
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-5828G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289275 | ||||||
| chr10:59289287
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02055.hp1 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.508-5840C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289287 | ||||||
| chr10:59289300
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.508-5853T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289300 | ||||||
| chr10:59289502
|
C | T | 1 | a0001c0004t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.508-6055G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289502 | ||||||
| chr10:59289644
|
C | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-6197G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289644 | ||||||
| chr10:59289785
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.508-6338C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289785 | ||||||
| chr10:59289801
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.508-6354C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289801 | ||||||
| chr10:59290081
|
T | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-6634A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290081 | ||||||
| chr10:59290554
|
C | A | 1 | a0001c0001t0001g0021 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.508-7107G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290554 | ||||||
| chr10:59290579
|
T | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(23): Show | 27 | HG01884.hp1 HG01891.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.508-7132A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290579 | ||||||
| chr10:59290867
|
G | T | 44 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0091others(41): Show | 44 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.508-7420C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290867 | ||||||
| chr10:59290893
|
A | G | 34 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0033others(31): Show | 34 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.508-7446T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290893 | ||||||
| chr10:59290966
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.508-7519G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290966 | ||||||
| chr10:59291024
|
G | T | 5 | a0001c0001t0001g0122a0001c0001t0001g0165a0001c0001t0001g0186others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-7577C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291024 | ||||||
| chr10:59291115
|
A | G | 55 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0091others(52): Show | 55 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.508-7668T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291115 | ||||||
| chr10:59291203
|
A | G | 12 | a0001c0001t0001g0045a0001c0001t0001g0150a0001c0001t0001g0153others(9): Show | 12 | HG00639.hp2 HG01106.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-7756T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291203 | ||||||
| chr10:59291291
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.508-7844C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291291 | ||||||
| chr10:59291411
|
T | G | 1 | a0001c0001t0002g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.508-7964A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291411 | ||||||
| chr10:59291439
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.508-7992G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291439 | ||||||
| chr10:59291516
|
G | A | 33 | a0001c0001t0001g0045a0001c0001t0001g0067a0001c0001t0001g0089others(30): Show | 33 | HG00639.hp1 HG01106.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.508-8069C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291516 | ||||||
| chr10:59291523
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.508-8076T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291523 | ||||||
| chr10:59291579
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-8132A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291579 | ||||||
| chr10:59291670
|
A | AG | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 161 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.508-8224dupC | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291670 | ||||||
| chr10:59291770
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.508-8323G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291770 | ||||||
| chr10:59291785
|
C | CT | 21 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(18): Show | 22 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.508-8339dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291785 | ||||||
| chr10:59291785
|
CT | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0025others(19): Show | 22 | HG00323.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.508-8339delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291785 | ||||||
| chr10:59291785
|
CTT | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 148 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.508-8340_508-8339d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291785 | ||||||
| chr10:59291785
|
CTTT | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG03704.hp1 HG03927.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-8341_508-8339d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291785 | ||||||
| chr10:59291870
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.508-8423C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291870 | ||||||
| chr10:59291902
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.508-8455G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291902 | ||||||
| chr10:59291953
|
G | T | 12 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(9): Show | 12 | HG00639.hp1 HG01243.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.508-8506C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291953 | ||||||
| chr10:59291972
|
T | C | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-8525A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291972 | ||||||
| chr10:59291977
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0201 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.508-8530C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291977 | ||||||
| chr10:59291979
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.508-8532T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291979 | ||||||
| chr10:59291989
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0137 | 2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.508-8542G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291989 | ||||||
| chr10:59291990
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0137 | 2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.508-8543T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291990 | ||||||
| chr10:59291992
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0137 | 2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.508-8545T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291992 | ||||||
| chr10:59292004
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-8557C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292004 | ||||||
| chr10:59292010
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0112others(2): Show | 5 | HG01433.hp2 HG03704.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-8563A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292010 | ||||||
| chr10:59292010
|
T | G | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.508-8563A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292010 | ||||||
| chr10:59292027
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.508-8580C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292027 | ||||||
| chr10:59292077
|
T | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 10 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-8630A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292077 | ||||||
| chr10:59292079
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.508-8632G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292079 | ||||||
| chr10:59292172
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.508-8725G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292172 | ||||||
| chr10:59292209
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.508-8762C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292209 | ||||||
| chr10:59292241
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.508-8794C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292241 | ||||||
| chr10:59292278
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0061others(28): Show | 31 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.508-8831G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292278 | ||||||
| chr10:59292309
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 201 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.508-8862G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292309 | ||||||
| chr10:59292363
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508-8916A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292363 | ||||||
| chr10:59292575
|
T | C | 18 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(15): Show | 18 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.508-9128A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292575 | ||||||
| chr10:59292947
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.508-9500A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292947 | ||||||
| chr10:59293069
|
C | CT | 24 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0032others(21): Show | 24 | HG00639.hp2 HG01106.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.508-9623dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293069 | ||||||
| chr10:59293069
|
C | CTT | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 97 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.508-9624_508-9623d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293069 | ||||||
| chr10:59293069
|
C | CTTT | 21 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0044others(18): Show | 21 | HG00735.hp2 HG01123.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.508-9625_508-9623d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293069 | ||||||
| chr10:59293069
|
CTTTTTTT others(3): Show |
C | 57 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0025others(54): Show | 57 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.508-9632_508-9623d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293069 | ||||||
| chr10:59293106
|
T | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0155a0001c0001t0001g0158others(1): Show | 4 | HG02970.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-9659A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293106 | ||||||
| chr10:59293198
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 201 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.507+9603A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293198 | ||||||
| chr10:59293240
|
A | AT | 57 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0025others(54): Show | 57 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.507+9560dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293240 | ||||||
| chr10:59293266
|
C | T | 1 | a0001c0001t0002g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.507+9535G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293266 | ||||||
| chr10:59293296
|
T | C | 8 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0070others(5): Show | 8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+9505A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293296 | ||||||
| chr10:59293371
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.507+9430G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293371 | ||||||
| chr10:59293588
|
T | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+9213A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293588 | ||||||
| chr10:59293661
|
C | A | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+9140G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293661 | ||||||
| chr10:59293676
|
A | G | 1 | a0002c0002t0001g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.507+9125T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293676 | ||||||
| chr10:59293770
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 201 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.507+9031C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293770 | ||||||
| chr10:59293820
|
C | A | 56 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0025others(53): Show | 56 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.507+8981G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293820 | ||||||
| chr10:59293879
|
T | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+8922A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293879 | ||||||
| chr10:59294095
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.507+8706G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294095 | ||||||
| chr10:59294123
|
TA | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0187a0001c0001t0001g0201 | 3 | HG01891.hp1 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.507+8677delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294123 | ||||||
| chr10:59294124
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.507+8677T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294124 | ||||||
| chr10:59294496
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0112a0001c0001t0001g0151 | 3 | HG01433.hp2 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.507+8305A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294496 | ||||||
| chr10:59294931
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.507+7870T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294931 | ||||||
| chr10:59295083
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.507+7718G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295083 | ||||||
| chr10:59295171
|
C | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+7630G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295171 | ||||||
| chr10:59295250
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(11): Show | 14 | HG00609.hp1 HG00673.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.507+7551T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295250 | ||||||
| chr10:59295336
|
G | A | 27 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(24): Show | 27 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+7465C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295336 | ||||||
| chr10:59295377
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.507+7424G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295377 | ||||||
| chr10:59295384
|
G | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0046others(5): Show | 8 | HG01123.hp1 HG02647.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+7417C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295384 | ||||||
| chr10:59295494
|
C | CTA | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+7306_507+7307i others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295494 | ||||||
| chr10:59295554
|
C | G | 2 | a0002c0002t0001g0037a0002c0002t0001g0095 | 2 | HG01243.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.507+7247G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295554 | ||||||
| chr10:59295709
|
C | A | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+7092G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295709 | ||||||
| chr10:59295817
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.507+6984A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295817 | ||||||
| chr10:59296123
|
T | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+6678A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296123 | ||||||
| chr10:59296371
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+6430T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296371 | ||||||
| chr10:59296390
|
C | A | 62 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0025others(59): Show | 62 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.507+6411G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296390 | ||||||
| chr10:59296624
|
T | A | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+6177A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296624 | ||||||
| chr10:59296707
|
T | G | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.507+6094A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296707 | ||||||
| chr10:59296743
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.507+6058G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296743 | ||||||
| chr10:59297082
|
C | T | 52 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0025others(49): Show | 52 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.507+5719G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297082 | ||||||
| chr10:59297083
|
G | A | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.507+5718C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297083 | ||||||
| chr10:59297212
|
C | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+5589G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297212 | ||||||
| chr10:59297536
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.507+5265A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297536 | ||||||
| chr10:59297551
|
C | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+5250G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297551 | ||||||
| chr10:59297580
|
G | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.507+5221C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297580 | ||||||
| chr10:59297676
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.507+5125C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297676 | ||||||
| chr10:59297744
|
A | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0046others(5): Show | 8 | HG01123.hp1 HG02647.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+5057T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297744 | ||||||
| chr10:59297873
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0153a0001c0001t0001g0187others(1): Show | 4 | HG01891.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+4928G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297873 | ||||||
| chr10:59297900
|
C | CA | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 93 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.507+4900dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297900 | ||||||
| chr10:59297943
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.507+4858A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297943 | ||||||
| chr10:59297949
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.507+4852G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297949 | ||||||
| chr10:59297953
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.507+4848T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297953 | ||||||
| chr10:59297976
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.507+4825G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297976 | ||||||
| chr10:59297992
|
A | G | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4809T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297992 | ||||||
| chr10:59298265
|
G | A | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4536C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298265 | ||||||
| chr10:59298273
|
T | C | 2 | a0001c0001t0001g0188a0001c0007t0001g0059 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.507+4528A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298273 | ||||||
| chr10:59298277
|
A | G | 27 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(24): Show | 27 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+4524T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298277 | ||||||
| chr10:59298409
|
G | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4392C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298409 | ||||||
| chr10:59298642
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.507+4159T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298642 | ||||||
| chr10:59298880
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.507+3921C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298880 | ||||||
| chr10:59299038
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 90 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.507+3763G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299038 | ||||||
| chr10:59299272
|
T | TA | 4 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0084others(1): Show | 4 | NA18942.hp1 NA18942.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+3528dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299272 | ||||||
| chr10:59299344
|
GC | G | 27 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(24): Show | 27 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+3456delG | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299344 | ||||||
| chr10:59299385
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.507+3416T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299385 | ||||||
| chr10:59299445
|
G | C | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+3356C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299445 | ||||||
| chr10:59299474
|
T | C | 2 | a0001c0001t0002g0090a0001c0001t0004g0128 | 2 | HG02300.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.507+3327A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299474 | ||||||
| chr10:59299511
|
C | CT | 6 | a0001c0001t0001g0067a0001c0001t0001g0091a0001c0001t0001g0112others(3): Show | 6 | HG01433.hp2 HG03453.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+3289dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299511 | ||||||
| chr10:59299511
|
CT | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0028others(23): Show | 26 | HG01106.hp1 HG01123.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.507+3289delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299511 | ||||||
| chr10:59299511
|
CTT | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+3288_507+3289d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299511 | ||||||
| chr10:59299545
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.507+3256G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299545 | ||||||
| chr10:59299610
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.507+3191T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299610 | ||||||
| chr10:59299696
|
G | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0046others(5): Show | 8 | HG01123.hp1 HG02647.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+3105C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299696 | ||||||
| chr10:59299904
|
A | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 149 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.507+2897T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299904 | ||||||
| chr10:59299987
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.507+2814T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299987 | ||||||
| chr10:59300052
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 89 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.507+2749C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300052 | ||||||
| chr10:59300077
|
A | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+2724T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300077 | ||||||
| chr10:59300313
|
T | G | 8 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0070others(5): Show | 8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+2488A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300313 | ||||||
| chr10:59300324
|
C | T | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+2477G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300324 | ||||||
| chr10:59300349
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0116 | 2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.507+2452G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300349 | ||||||
| chr10:59300536
|
G | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+2265C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300536 | ||||||
| chr10:59300635
|
C | G | 8 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0070others(5): Show | 8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+2166G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300635 | ||||||
| chr10:59300655
|
G | C | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.507+2146C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300655 | ||||||
| chr10:59300683
|
C | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.507+2118G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300683 | ||||||
| chr10:59300808
|
C | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0070others(5): Show | 8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+1993G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300808 | ||||||
| chr10:59300812
|
T | C | 2 | a0004c0005t0001g0027a0004c0005t0001g0149 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+1989A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300812 | ||||||
| chr10:59300919
|
C | T | 27 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(24): Show | 27 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+1882G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300919 | ||||||
| chr10:59300922
|
T | C | 12 | a0001c0001t0001g0122a0001c0001t0001g0178a0001c0001t0001g0180others(9): Show | 12 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+1879A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300922 | ||||||
| chr10:59301032
|
A | G | 44 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(41): Show | 44 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.507+1769T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301032 | ||||||
| chr10:59301068
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+1733A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301068 | ||||||
| chr10:59301269
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.507+1532A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301269 | ||||||
| chr10:59301324
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.507+1477T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301324 | ||||||
| chr10:59301595
|
T | TA | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0046others(9): Show | 12 | HG01123.hp1 HG02486.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+1205dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301595 | ||||||
| chr10:59301613
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.507+1188G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301613 | ||||||
| chr10:59301690
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.507+1111G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301690 | ||||||
| chr10:59301727
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 153 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.507+1074T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301727 | ||||||
| chr10:59301747
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.507+1054T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301747 | ||||||
| chr10:59301829
|
T | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0112a0001c0001t0001g0151others(2): Show | 5 | HG01433.hp2 HG03453.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+972A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301829 | ||||||
| chr10:59301983
|
G | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0070others(5): Show | 8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+818C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301983 | ||||||
| chr10:59302008
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.507+793C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59302008 | ||||||
| chr10:59302025
|
CG | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.507+775delC | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59302025 | ||||||
| chr10:59302032
|
GC | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.507+768delG | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59302032 | ||||||
| chr10:59302625
|
C | T | 4 | a0003c0003t0001g0192a0003c0003t0001g0193a0003c0003t0001g0194others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+176G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59302625 | ||||||
| chr10:59302778
|
T | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+23A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59302778 | ||||||
| chr10:59303134
|
A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0046others(9): Show | 12 | HG01123.hp1 HG02486.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.444-270T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303134 | ||||||
| chr10:59303214
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444-350T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303214 | ||||||
| chr10:59303254
|
G | A | 28 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(25): Show | 28 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.444-390C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303254 | ||||||
| chr10:59303397
|
A | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 154 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.444-533T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303397 | ||||||
| chr10:59303515
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.444-651T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303515 | ||||||
| chr10:59303568
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.444-704G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303568 | ||||||
| chr10:59303860
|
G | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0127a0001c0001t0001g0129 | 3 | HG00738.hp2 HG01081.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.444-996C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303860 | ||||||
| chr10:59303934
|
G | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0102a0001c0001t0001g0167 | 3 | HG01081.hp1 HG01106.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.444-1070C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303934 | ||||||
| chr10:59304009
|
G | A | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.444-1145C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304009 | ||||||
| chr10:59304105
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0112a0001c0001t0001g0151 | 3 | HG01433.hp2 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.444-1241C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304105 | ||||||
| chr10:59304129
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.444-1265G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304129 | ||||||
| chr10:59304547
|
C | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.444-1683G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304547 | ||||||
| chr10:59304761
|
G | GAGGGA | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(41): Show | 44 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.444-1902_444-1898d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(3): Show |
33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(30): Show | 33 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.444-1907_444-1898d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(8): Show |
13 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0039others(10): Show | 13 | HG01099.hp1 HG01099.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.444-1912_444-1898d others(17): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(13): Show |
10 | a0001c0001t0001g0025a0001c0001t0001g0152a0001c0001t0001g0175others(7): Show | 10 | HG00738.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.444-1917_444-1898d others(22): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(18): Show |
22 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0070others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.444-1922_444-1898d others(27): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(23): Show |
20 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(17): Show | 20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.444-1898_444-1897i others(32): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(23): Show |
18 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0054others(15): Show | 19 | HG00558.hp2 HG01106.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.444-1927_444-1898d others(32): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(28): Show |
11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0092others(8): Show | 11 | HG00639.hp1 HG00673.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.444-1932_444-1898d others(37): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(33): Show |
4 | a0001c0001t0001g0051a0003c0003t0001g0192a0003c0003t0001g0193others(1): Show | 4 | HG01243.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-1937_444-1898d others(42): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
G | GAGGGAAG others(43): Show |
1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.444-1947_444-1898d others(52): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304761
|
GAGGGA | G | 2 | a0001c0001t0001g0189a0001c0001t0007g0185 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.444-1902_444-1898d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | ||||||
| chr10:59304786
|
A | AAAGGAAG others(23): Show |
1 | a0001c0001t0001g0073 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.444-1923_444-1922i others(32): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304786 | ||||||
| chr10:59304798
|
G | GGGAAGGG others(2): Show |
4 | a0001c0001t0001g0011a0001c0001t0001g0072a0001c0001t0001g0116others(1): Show | 4 | HG00609.hp1 HG00673.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1943_444-1935d others(11): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304798 | ||||||
| chr10:59304810
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.444-1946C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304810 | ||||||
| chr10:59304815
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0139 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.444-1951T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304815 | ||||||
| chr10:59304823
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.444-1959T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304823 | ||||||
| chr10:59304828
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.444-1964T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304828 | ||||||
| chr10:59304834
|
C | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0173 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.444-1970G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304834 | ||||||
| chr10:59304834
|
C | CGGGGGA | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.444-1976_444-1971d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304834 | ||||||
| chr10:59304847
|
G | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1983C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304847 | ||||||
| chr10:59304852
|
A | C | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444-1988T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304852 | ||||||
| chr10:59304857
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444-1993T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304857 | ||||||
| chr10:59304862
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444-1998T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304862 | ||||||
| chr10:59304863
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444-1999T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304863 | ||||||
| chr10:59304869
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(73): Show | 77 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.444-2005C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304869 | ||||||
| chr10:59304895
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 31 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.444-2031A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304895 | ||||||
| chr10:59304906
|
G | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(11): Show | 14 | HG00609.hp1 HG00673.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.444-2042C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304906 | ||||||
| chr10:59305123
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.444-2259G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305123 | ||||||
| chr10:59305202
|
A | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.444-2338T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305202 | ||||||
| chr10:59305226
|
G | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.444-2362C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305226 | ||||||
| chr10:59305408
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(25): Show | 29 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.444-2544C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305408 | ||||||
| chr10:59305438
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0112 | 2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.444-2574A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305438 | ||||||
| chr10:59305520
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.444-2656T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305520 | ||||||
| chr10:59305628
|
AT | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0042others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.444-2765delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305628 | ||||||
| chr10:59305682
|
A | C | 6 | a0001c0001t0001g0091a0001c0001t0001g0153a0001c0001t0001g0187others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.444-2818T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305682 | ||||||
| chr10:59306012
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 201 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.444-3148T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306012 | ||||||
| chr10:59306175
|
G | C | 3 | a0001c0001t0001g0147a0001c0001t0002g0008a0006c0009t0001g0142 | 3 | HG01261.hp2 HG03540.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.444-3311C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306175 | ||||||
| chr10:59306255
|
G | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.444-3391C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306255 | ||||||
| chr10:59306437
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.444-3573C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306437 | ||||||
| chr10:59306544
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.444-3680T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306544 | ||||||
| chr10:59306554
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0099others(1): Show | 4 | HG01071.hp2 HG02135.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-3690C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306554 | ||||||
| chr10:59306559
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.444-3695T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306559 | ||||||
| chr10:59306573
|
G | C | 1 | a0001c0001t0001g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.444-3709C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306573 | ||||||
| chr10:59306676
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 89 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.444-3812C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306676 | ||||||
| chr10:59306684
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444-3820A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306684 | ||||||
| chr10:59306903
|
G | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.444-4039C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306903 | ||||||
| chr10:59306974
|
G | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(64): Show | 67 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.444-4110C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306974 | ||||||
| chr10:59307105
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.444-4241C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307105 | ||||||
| chr10:59307328
|
C | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.444-4464G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307328 | ||||||
| chr10:59307468
|
T | C | 6 | a0001c0001t0001g0091a0001c0001t0001g0153a0001c0001t0001g0187others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.444-4604A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307468 | ||||||
| chr10:59307483
|
C | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-4619G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307483 | ||||||
| chr10:59307585
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.444-4721C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307585 | ||||||
| chr10:59307641
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.444-4777A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307641 | ||||||
| chr10:59307667
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0153a0001c0001t0001g0187others(1): Show | 4 | HG01891.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-4803C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307667 | ||||||
| chr10:59307674
|
T | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.444-4810A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307674 | ||||||
| chr10:59307793
|
C | A | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.444-4929G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307793 | ||||||
| chr10:59307820
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.444-4956A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307820 | ||||||
| chr10:59308198
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.444-5334C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308198 | ||||||
| chr10:59308198
|
G | C | 4 | a0001c0001t0001g0191a0001c0001t0003g0018a0001c0001t0003g0171others(1): Show | 4 | HG00639.hp2 HG02145.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-5334C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308198 | ||||||
| chr10:59308344
|
A | T | 5 | a0001c0001t0001g0165a0001c0001t0001g0172a0001c0001t0001g0186others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-5480T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308344 | ||||||
| chr10:59308365
|
A | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0098others(1): Show | 5 | NA18941.hp2 NA18947.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.444-5501T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308365 | ||||||
| chr10:59308372
|
C | T | 5 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0003g0018others(2): Show | 5 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-5508G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308372 | ||||||
| chr10:59308566
|
C | CCACCATC others(27): Show |
103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 104 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.444-5736_444-5703d others(36): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308566 | ||||||
| chr10:59308606
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0106 | 3 | HG02004.hp2 NA18965.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.444-5742A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308606 | ||||||
| chr10:59308762
|
C | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(19): Show | 22 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.444-5898G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308762 | ||||||
| chr10:59308886
|
G | A | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.444-6022C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308886 | ||||||
| chr10:59309063
|
A | G | 5 | a0001c0001t0001g0165a0001c0001t0001g0172a0001c0001t0001g0186others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-6199T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309063 | ||||||
| chr10:59309114
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.444-6250C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309114 | ||||||
| chr10:59309123
|
G | T | 11 | a0001c0001t0001g0165a0001c0001t0001g0172a0001c0001t0001g0174others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.444-6259C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309123 | ||||||
| chr10:59309137
|
C | T | 15 | a0001c0001t0001g0085a0001c0001t0001g0165a0001c0001t0001g0172others(12): Show | 15 | HG00639.hp2 HG02257.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.444-6273G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309137 | ||||||
| chr10:59309343
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.444-6479G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309343 | ||||||
| chr10:59309418
|
T | C | 3 | a0001c0001t0001g0173a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02965.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444-6554A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309418 | ||||||
| chr10:59309451
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 112 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.444-6587G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309451 | ||||||
| chr10:59309649
|
T | C | 2 | a0001c0001t0001g0070a0002c0002t0006g0198 | 2 | HG01123.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.444-6785A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309649 | ||||||
| chr10:59309822
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.444-6958G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309822 | ||||||
| chr10:59309846
|
T | C | 1 | a0001c0004t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.444-6982A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309846 | ||||||
| chr10:59309885
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.444-7021T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309885 | ||||||
| chr10:59309927
|
TA | T | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-7064delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309927 | ||||||
| chr10:59309950
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0007c0010t0001g0148 | 3 | HG00639.hp2 HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.444-7086A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309950 | ||||||
| chr10:59310148
|
G | A | 2 | a0001c0001t0001g0070a0002c0002t0006g0198 | 2 | HG01123.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.444-7284C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310148 | ||||||
| chr10:59310160
|
C | G | 1 | a0001c0001t0002g0079 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.444-7296G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310160 | ||||||
| chr10:59310317
|
A | G | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-7453T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310317 | ||||||
| chr10:59310807
|
T | G | 37 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0070others(34): Show | 37 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.444-7943A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310807 | ||||||
| chr10:59310840
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0155a0001c0001t0001g0158others(1): Show | 4 | HG02970.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-7976G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310840 | ||||||
| chr10:59311067
|
A | G | 37 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0070others(34): Show | 37 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.444-8203T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59311067 | ||||||
| chr10:59311237
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.444-8373G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59311237 | ||||||
| chr10:59311928
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.444-9064G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59311928 | ||||||
| chr10:59311991
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0070 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.444-9127G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59311991 | ||||||
| chr10:59312139
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 109 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.444-9275G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312139 | ||||||
| chr10:59312146
|
T | G | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-9282A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312146 | ||||||
| chr10:59312173
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0049others(4): Show | 7 | HG00639.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.444-9309G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312173 | ||||||
| chr10:59312297
|
G | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0049others(1): Show | 4 | HG02897.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-9433C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312297 | ||||||
| chr10:59312326
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.444-9462C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312326 | ||||||
| chr10:59312373
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.444-9509T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312373 | ||||||
| chr10:59312422
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.444-9558A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312422 | ||||||
| chr10:59312423
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.444-9559G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312423 | ||||||
| chr10:59312489
|
A | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0202others(1): Show | 4 | HG01167.hp1 HG02622.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-9625T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312489 | ||||||
| chr10:59312596
|
C | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0061others(31): Show | 34 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.444-9732G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312596 | ||||||
| chr10:59312886
|
A | C | 1 | a0001c0001t0002g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.444-10022T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312886 | ||||||
| chr10:59312929
|
T | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0061others(32): Show | 35 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.444-10065A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312929 | ||||||
| chr10:59312994
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.444-10130G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312994 | ||||||
| chr10:59313108
|
G | C | 33 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.444-10244C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313108 | ||||||
| chr10:59313134
|
G | A | 11 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0200others(8): Show | 11 | HG01123.hp1 HG01167.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.444-10270C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313134 | ||||||
| chr10:59313213
|
T | C | 7 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0189others(4): Show | 7 | HG00639.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.444-10349A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313213 | ||||||
| chr10:59313281
|
G | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-10417C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313281 | ||||||
| chr10:59313497
|
G | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.443+10491C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313497 | ||||||
| chr10:59313570
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.443+10418G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313570 | ||||||
| chr10:59313573
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.443+10415C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313573 | ||||||
| chr10:59313622
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG00609.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.443+10366C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313622 | ||||||
| chr10:59313685
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0159 | 2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.443+10303A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313685 | ||||||
| chr10:59313726
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.443+10262C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313726 | ||||||
| chr10:59313841
|
G | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0197others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+10147C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313841 | ||||||
| chr10:59313854
|
A | G | 33 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.443+10134T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313854 | ||||||
| chr10:59314217
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.443+9771T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314217 | ||||||
| chr10:59314249
|
G | A | 4 | a0001c0001t0001g0174a0002c0002t0001g0017a0002c0002t0001g0035others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+9739C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314249 | ||||||
| chr10:59314260
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.443+9728G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314260 | ||||||
| chr10:59314284
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.443+9704T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314284 | ||||||
| chr10:59314296
|
C | G | 33 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0152others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.443+9692G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314296 | ||||||
| chr10:59314351
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.443+9637G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314351 | ||||||
| chr10:59314887
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0118 | 2 | HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.443+9101T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314887 | ||||||
| chr10:59315203
|
G | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0106a0001c0001t0002g0081 | 3 | HG00597.hp2 NA18942.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.443+8785C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315203 | ||||||
| chr10:59315419
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.443+8569T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315419 | ||||||
| chr10:59315445
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0196 | 2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.443+8543C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315445 | ||||||
| chr10:59315446
|
G | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.443+8542C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315446 | ||||||
| chr10:59315453
|
T | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(137): Show | 140 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.443+8535A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315453 | ||||||
| chr10:59315483
|
T | C | 5 | a0001c0001t0001g0092a0003c0003t0001g0192a0003c0003t0001g0193others(2): Show | 5 | HG00639.hp1 HG01243.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+8505A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315483 | ||||||
| chr10:59315499
|
T | G | 1 | a0001c0001t0002g0065 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.443+8489A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315499 | ||||||
| chr10:59315515
|
G | T | 15 | a0001c0001t0001g0043a0001c0001t0001g0152a0001c0001t0001g0158others(12): Show | 15 | HG00738.hp1 HG02257.hp1 HG02683.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+8473C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315515 | ||||||
| chr10:59315689
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0179 | 3 | HG01070.hp1 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.443+8299G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315689 | ||||||
| chr10:59315849
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.443+8139A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315849 | ||||||
| chr10:59315898
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.443+8090T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315898 | ||||||
| chr10:59315913
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0165a0001c0001t0001g0196 | 3 | HG02257.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.443+8075G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315913 | ||||||
| chr10:59315997
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 38 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.443+7991A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315997 | ||||||
| chr10:59316040
|
ATG | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 99 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.443+7946_443+7947d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316040 | ||||||
| chr10:59316077
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(24): Show | 27 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.443+7911C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316077 | ||||||
| chr10:59316235
|
G | T | 1 | a0001c0001t0002g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.443+7753C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316235 | ||||||
| chr10:59316415
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(6): Show | 9 | HG02486.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.443+7573T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316415 | ||||||
| chr10:59316513
|
T | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0132 | 2 | NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.443+7475A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316513 | ||||||
| chr10:59316599
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+7389C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316599 | ||||||
| chr10:59316712
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.443+7276C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316712 | ||||||
| chr10:59316718
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 193 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.443+7270G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316718 | ||||||
| chr10:59316819
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.443+7169C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316819 | ||||||
| chr10:59316864
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0165a0001c0001t0001g0196 | 3 | HG02257.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.443+7124T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316864 | ||||||
| chr10:59316976
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.443+7012A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316976 | ||||||
| chr10:59317126
|
A | ATG | 19 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 19 | HG00735.hp1 HG01071.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.443+6860_443+6861d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | ||||||
| chr10:59317126
|
A | ATGTG | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 76 | HG00323.hp2 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.443+6858_443+6861d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | ||||||
| chr10:59317126
|
A | ATGTGTG | 5 | a0001c0001t0001g0012a0001c0001t0001g0084a0001c0001t0001g0106others(2): Show | 5 | HG00597.hp2 HG03225.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+6856_443+6861d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | ||||||
| chr10:59317126
|
ATG | A | 73 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0030others(70): Show | 73 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.443+6860_443+6861d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | ||||||
| chr10:59317126
|
ATGTG | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0070a0001c0001t0001g0139others(2): Show | 5 | HG02280.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+6858_443+6861d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | ||||||
| chr10:59317228
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.443+6760G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317228 | ||||||
| chr10:59317558
|
A | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+6430T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317558 | ||||||
| chr10:59317589
|
C | A | 1 | a0001c0004t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.443+6399G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317589 | ||||||
| chr10:59317653
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.443+6335G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317653 | ||||||
| chr10:59317781
|
A | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 95 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.443+6207T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317781 | ||||||
| chr10:59317837
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 95 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.443+6151C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317837 | ||||||
| chr10:59317861
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+6127C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317861 | ||||||
| chr10:59318005
|
C | T | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+5983G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318005 | ||||||
| chr10:59318076
|
G | A | 6 | a0002c0002t0001g0017a0002c0002t0001g0035a0002c0002t0001g0036others(3): Show | 6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+5912C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318076 | ||||||
| chr10:59318192
|
T | TCTAAGTT others(327): Show |
3 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG01167.hp1 HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.443+5795_443+5796i others(336): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318192 | ||||||
| chr10:59318192
|
T | TCTAAGTT others(328): Show |
2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.443+5795_443+5796i others(337): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318192 | ||||||
| chr10:59318193
|
C | T | 6 | a0002c0002t0001g0017a0002c0002t0001g0035a0002c0002t0001g0036others(3): Show | 6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+5795G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318193 | ||||||
| chr10:59318273
|
TA | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 135 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.443+5714delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318273 | ||||||
| chr10:59318284
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+5704G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318284 | ||||||
| chr10:59318346
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 135 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.443+5642G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318346 | ||||||
| chr10:59318349
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 95 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.443+5639C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318349 | ||||||
| chr10:59318685
|
TGAA | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 95 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.443+5300_443+5302d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318685 | ||||||
| chr10:59318850
|
A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(9): Show | 12 | HG00639.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.443+5138T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318850 | ||||||
| chr10:59319072
|
A | AAC | 22 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0040others(19): Show | 22 | HG01099.hp1 HG01243.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.443+4914_443+4915d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
A | AACAC | 3 | a0001c0001t0001g0129a0001c0001t0001g0190a0001c0004t0001g0100 | 3 | HG01168.hp1 HG01891.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.443+4912_443+4915d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
A | AACACAC | 3 | a0001c0001t0002g0075a0001c0004t0001g0048a0002c0002t0006g0198 | 3 | HG01123.hp1 HG02630.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.443+4910_443+4915d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
AAC | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(41): Show | 45 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.443+4914_443+4915d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
AACAC | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0030others(11): Show | 14 | HG00323.hp2 HG00673.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.443+4912_443+4915d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
AACACAC | A | 9 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0096others(6): Show | 9 | HG00558.hp1 HG01123.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.443+4910_443+4915d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
AACACACA others(1): Show |
A | 14 | a0001c0001t0001g0054a0001c0001t0001g0070a0001c0001t0001g0073others(11): Show | 14 | HG00735.hp2 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.443+4908_443+4915d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
AACACACA others(3): Show |
A | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.443+4906_443+4915d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
AACACACA others(5): Show |
A | 2 | a0001c0001t0001g0154a0001c0007t0001g0059 | 2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.443+4904_443+4915d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319072
|
AACACACA others(9): Show |
A | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.443+4900_443+4915d others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | ||||||
| chr10:59319103
|
ACACACAC others(11): Show |
A | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+4867_443+4884d others(20): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319103 | ||||||
| chr10:59319107
|
ACACACAC others(7): Show |
A | 4 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+4867_443+4880d others(16): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319107 | ||||||
| chr10:59319109
|
ACACACAC others(5): Show |
A | 2 | a0001c0001t0001g0007a0001c0001t0001g0188 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.443+4867_443+4878d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319109 | ||||||
| chr10:59319113
|
ACACACAT others(1): Show |
A | 2 | a0001c0001t0001g0025a0001c0001t0001g0197 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.443+4867_443+4874d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319113 | ||||||
| chr10:59319117
|
ACATT | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0199 | 2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.443+4867_443+4870d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319117 | ||||||
| chr10:59319120
|
T | C | 7 | a0001c0001t0001g0186a0002c0002t0001g0017a0002c0002t0001g0035others(4): Show | 7 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.443+4868A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319120 | ||||||
| chr10:59319121
|
T | A | 7 | a0001c0001t0001g0186a0002c0002t0001g0017a0002c0002t0001g0035others(4): Show | 7 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.443+4867A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319121 | ||||||
| chr10:59319171
|
T | C | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.443+4817A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319171 | ||||||
| chr10:59319267
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.443+4721G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319267 | ||||||
| chr10:59319439
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443+4549C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319439 | ||||||
| chr10:59319541
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.443+4447G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319541 | ||||||
| chr10:59319546
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0007g0185 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.443+4442T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319546 | ||||||
| chr10:59319595
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+4393C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319595 | ||||||
| chr10:59320000
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443+3988T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320000 | ||||||
| chr10:59320578
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+3410G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320578 | ||||||
| chr10:59320729
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0002g0090 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.443+3259A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320729 | ||||||
| chr10:59320860
|
G | T | 5 | a0001c0001t0001g0054a0001c0001t0001g0091a0001c0001t0001g0165others(2): Show | 5 | HG02257.hp2 HG02922.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+3128C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320860 | ||||||
| chr10:59320876
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.443+3112A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320876 | ||||||
| chr10:59321059
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443+2929T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321059 | ||||||
| chr10:59321207
|
AT | A | 5 | a0002c0002t0001g0017a0002c0002t0001g0035a0002c0002t0001g0036others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+2780delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321207 | ||||||
| chr10:59321430
|
AC | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0061a0001c0001t0001g0097others(3): Show | 6 | HG02109.hp2 HG02135.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+2557delG | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321430 | ||||||
| chr10:59321431
|
C | CTT | 2 | a0001c0001t0001g0054a0001c0001t0001g0172 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.443+2556_443+2557i others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | ||||||
| chr10:59321431
|
CCT | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(25): Show | 29 | HG00323.hp2 HG00609.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.443+2555_443+2556d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | ||||||
| chr10:59321431
|
CCTT | C | 31 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 31 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.443+2554_443+2556d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | ||||||
| chr10:59321431
|
CCTTT | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0049others(14): Show | 17 | HG00639.hp1 HG01070.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.443+2553_443+2556d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | ||||||
| chr10:59321431
|
CCTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.443+2546_443+2556d others(13): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | ||||||
| chr10:59321431
|
CCTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.443+2544_443+2556d others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | ||||||
| chr10:59321432
|
C | CT | 28 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0039others(25): Show | 28 | HG00558.hp1 HG00609.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.443+2555dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | ||||||
| chr10:59321432
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0040others(4): Show | 7 | HG01099.hp1 HG01099.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+2556G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | ||||||
| chr10:59321432
|
CTTTT | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0200others(2): Show | 5 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+2552_443+2555d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | ||||||
| chr10:59321432
|
CTTTTT | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0093others(3): Show | 6 | HG02451.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+2551_443+2555d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | ||||||
| chr10:59321432
|
CTTTTTTT | C | 8 | a0001c0001t0001g0153a0001c0001t0001g0186a0002c0002t0001g0017others(5): Show | 8 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.443+2549_443+2555d others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | ||||||
| chr10:59321441
|
T | C | 4 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01106.hp1 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.443+2547A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321441 | ||||||
| chr10:59321461
|
G | A | 6 | a0002c0002t0001g0017a0002c0002t0001g0035a0002c0002t0001g0036others(3): Show | 6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+2527C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321461 | ||||||
| chr10:59321664
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(83): Show | 87 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.443+2324T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321664 | ||||||
| chr10:59321694
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.443+2294C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321694 | ||||||
| chr10:59321715
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.443+2273G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321715 | ||||||
| chr10:59321846
|
A | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+2142T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321846 | ||||||
| chr10:59321853
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.443+2135G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321853 | ||||||
| chr10:59321953
|
A | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 118 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.443+2035T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321953 | ||||||
| chr10:59322014
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.443+1974G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322014 | ||||||
| chr10:59322059
|
T | A | 15 | a0001c0001t0001g0070a0001c0001t0001g0122a0001c0001t0001g0154others(12): Show | 15 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+1929A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322059 | ||||||
| chr10:59322204
|
AT | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(84): Show | 88 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.443+1783delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322204 | ||||||
| chr10:59322232
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443+1756G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322232 | ||||||
| chr10:59322303
|
A | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+1685T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322303 | ||||||
| chr10:59322308
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 95 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.443+1680G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322308 | ||||||
| chr10:59322583
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 96 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.443+1405G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322583 | ||||||
| chr10:59322912
|
C | A | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.443+1076G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322912 | ||||||
| chr10:59323022
|
T | G | 11 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(8): Show | 11 | HG00639.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.443+966A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323022 | ||||||
| chr10:59323242
|
C | A | 6 | a0002c0002t0001g0017a0002c0002t0001g0035a0002c0002t0001g0036others(3): Show | 6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+746G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323242 | ||||||
| chr10:59323457
|
C | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+531G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323457 | ||||||
| chr10:59323522
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.443+466T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323522 | ||||||
| chr10:59323557
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+431C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323557 | ||||||
| chr10:59323619
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.443+369T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323619 | ||||||
| chr10:59323722
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.443+266G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323722 | ||||||
| chr10:59323906
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.443+82G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323906 | ||||||
| chr10:59323930
|
A | AGTTG | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 118 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.443+57_443+58insCA others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323930 | ||||||
| chr10:59324184
|
C | G | 1 | a0001c0001t0001g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.325-78G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324184 | ||||||
| chr10:59324318
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0188 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.325-212G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324318 | ||||||
| chr10:59324408
|
G | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 95 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.325-302C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324408 | ||||||
| chr10:59324455
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.325-349T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324455 | ||||||
| chr10:59324508
|
T | TCA | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-404_325-403dup others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324508 | ||||||
| chr10:59324526
|
A | C | 1 | a0001c0001t0002g0124 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.325-420T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324526 | ||||||
| chr10:59324538
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 95 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.325-432A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324538 | ||||||
| chr10:59324550
|
A | C | 1 | a0001c0001t0001g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.325-444T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324550 | ||||||
| chr10:59324607
|
T | G | 3 | a0001c0001t0001g0154a0001c0004t0001g0100a0001c0007t0001g0059 | 3 | HG01891.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.325-501A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324607 | ||||||
| chr10:59324663
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 118 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-557T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324663 | ||||||
| chr10:59324902
|
A | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-796T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324902 | ||||||
| chr10:59324906
|
CAAAACT | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.325-806_325-801del others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324906 | ||||||
| chr10:59324983
|
G | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0129a0001c0001t0001g0136others(2): Show | 5 | HG01106.hp2 HG01168.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-877C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324983 | ||||||
| chr10:59325064
|
TAATAAAT others(15): Show |
T | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.325-980_325-959del others(22): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325064 | ||||||
| chr10:59325095
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.325-989C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325095 | ||||||
| chr10:59325125
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.325-1019A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325125 | ||||||
| chr10:59325128
|
T | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.325-1022A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325128 | ||||||
| chr10:59325322
|
C | T | 67 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(64): Show | 67 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.325-1216G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325322 | ||||||
| chr10:59325371
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.325-1265C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325371 | ||||||
| chr10:59325379
|
G | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-1273C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325379 | ||||||
| chr10:59325474
|
C | A | 5 | a0002c0002t0001g0017a0002c0002t0001g0035a0002c0002t0001g0036others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-1368G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325474 | ||||||
| chr10:59325482
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.325-1376T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325482 | ||||||
| chr10:59325503
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.325-1397C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325503 | ||||||
| chr10:59325522
|
C | T | 1 | a0001c0004t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.325-1416G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325522 | ||||||
| chr10:59325569
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 118 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-1463G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325569 | ||||||
| chr10:59325645
|
C | T | 5 | a0002c0002t0001g0017a0002c0002t0001g0035a0002c0002t0001g0036others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-1539G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325645 | ||||||
| chr10:59325895
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.325-1789T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325895 | ||||||
| chr10:59325944
|
G | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(7): Show | 10 | HG00639.hp2 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-1838C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325944 | ||||||
| chr10:59326450
|
G | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 186 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.325-2344C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59326450 | ||||||
| chr10:59326528
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0196 | 2 | HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.325-2422G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59326528 | ||||||
| chr10:59326684
|
G | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 119 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.325-2578C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59326684 | ||||||
| chr10:59326818
|
T | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-2712A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59326818 | ||||||
| chr10:59327349
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325-3243C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327349 | ||||||
| chr10:59327536
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 123 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.325-3430C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327536 | ||||||
| chr10:59327572
|
CA | C | 31 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0092others(28): Show | 31 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.325-3467delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327572 | ||||||
| chr10:59327573
|
A | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 92 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.325-3467T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327573 | ||||||
| chr10:59327575
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | HG02809.hp2 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-3469G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327575 | ||||||
| chr10:59327575
|
C | CA | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(56): Show | 60 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.325-3470dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327575 | ||||||
| chr10:59327575
|
C | CCA | 11 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0055others(8): Show | 11 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-3470_325-3469i others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327575 | ||||||
| chr10:59327575
|
C | CCCA | 7 | a0001c0001t0001g0023a0001c0001t0001g0050a0001c0001t0001g0076others(4): Show | 7 | HG01071.hp1 HG02004.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-3470_325-3469i others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327575 | ||||||
| chr10:59327661
|
C | T | 9 | a0001c0001t0001g0092a0001c0001t0001g0153a0001c0001t0001g0191others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-3555G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327661 | ||||||
| chr10:59327675
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 137 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.325-3569C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327675 | ||||||
| chr10:59327686
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.325-3580A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327686 | ||||||
| chr10:59327714
|
C | T | 4 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01106.hp1 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-3608G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327714 | ||||||
| chr10:59327937
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.325-3831C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327937 | ||||||
| chr10:59327998
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0122 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.325-3892G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327998 | ||||||
| chr10:59328008
|
A | G | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-3902T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328008 | ||||||
| chr10:59328039
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.325-3933G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328039 | ||||||
| chr10:59328152
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-4046A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328152 | ||||||
| chr10:59328154
|
T | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 128 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.325-4048A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328154 | ||||||
| chr10:59328191
|
T | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-4085A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328191 | ||||||
| chr10:59328487
|
A | AAAAAC | 30 | a0001c0001t0001g0007a0001c0001t0001g0092a0001c0001t0001g0153others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.325-4386_325-4382d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328487 | ||||||
| chr10:59328487
|
AAAAAC | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-4386_325-4382d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328487 | ||||||
| chr10:59328487
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.325-4391_325-4382d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328487 | ||||||
| chr10:59328502
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.325-4396G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328502 | ||||||
| chr10:59328521
|
A | T | 34 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.325-4415T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328521 | ||||||
| chr10:59328647
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325-4541T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328647 | ||||||
| chr10:59329165
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.325-5059T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329165 | ||||||
| chr10:59329232
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.325-5126C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329232 | ||||||
| chr10:59329280
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 83 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.325-5174T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329280 | ||||||
| chr10:59329342
|
GTT | G | 28 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0069others(25): Show | 28 | HG00323.hp1 HG00597.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.325-5238_325-5237d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTT | G | 29 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(26): Show | 29 | HG00558.hp1 HG00609.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.325-5239_325-5237d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTTTTTT others(2): Show |
G | 5 | a0001c0001t0001g0122a0001c0001t0001g0164a0001c0001t0001g0180others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-5245_325-5237d others(11): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTTTTTT others(3): Show |
G | 9 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0070others(6): Show | 9 | HG02280.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-5246_325-5237d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTTTTTT others(4): Show |
G | 13 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.325-5247_325-5237d others(13): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTTTTTT others(5): Show |
G | 12 | a0001c0001t0001g0007a0001c0001t0001g0092a0001c0001t0001g0153others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.325-5248_325-5237d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTTTTTT others(6): Show |
G | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.325-5249_325-5237d others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0001g0073 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.325-5254_325-5237d others(20): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTTTTTT others(12): Show |
G | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(83): Show | 87 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.325-5255_325-5237d others(21): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329342
|
GTTTTTTT others(13): Show |
G | 6 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0091others(3): Show | 6 | HG01070.hp2 HG02257.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-5256_325-5237d others(22): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | ||||||
| chr10:59329448
|
G | T | 34 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.325-5342C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329448 | ||||||
| chr10:59329550
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 94 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.325-5444T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329550 | ||||||
| chr10:59329582
|
CTCCTGAC others(9): Show |
C | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-5492_325-5477d others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329582 | ||||||
| chr10:59329586
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.325-5480A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329586 | ||||||
| chr10:59329615
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.325-5509G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329615 | ||||||
| chr10:59329650
|
G | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0007g0185 | 3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.325-5544C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329650 | ||||||
| chr10:59329697
|
T | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.325-5591A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329697 | ||||||
| chr10:59329707
|
G | A | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.325-5601C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329707 | ||||||
| chr10:59329745
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.325-5639A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329745 | ||||||
| chr10:59330026
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.325-5920C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330026 | ||||||
| chr10:59330101
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.325-5995C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330101 | ||||||
| chr10:59330243
|
T | G | 1 | a0001c0001t0002g0014 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.325-6137A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330243 | ||||||
| chr10:59330303
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-6197A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330303 | ||||||
| chr10:59330400
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0002g0081 | 2 | HG00597.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.325-6294C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330400 | ||||||
| chr10:59330591
|
A | T | 20 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0092others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.325-6485T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330591 | ||||||
| chr10:59330753
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 127 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.325-6647C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330753 | ||||||
| chr10:59330899
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 189 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.325-6793G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330899 | ||||||
| chr10:59331108
|
G | T | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.325-7002C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331108 | ||||||
| chr10:59331116
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-7010A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331116 | ||||||
| chr10:59331149
|
G | C | 1 | a0001c0001t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.325-7043C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331149 | ||||||
| chr10:59331232
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 122 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.325-7126A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331232 | ||||||
| chr10:59331243
|
G | T | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-7137C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331243 | ||||||
| chr10:59331321
|
C | T | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0153others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-7215G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331321 | ||||||
| chr10:59331403
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.325-7297G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331403 | ||||||
| chr10:59331409
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.325-7303C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331409 | ||||||
| chr10:59331542
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325-7436A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331542 | ||||||
| chr10:59331598
|
C | T | 6 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG03492.hp1 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-7492G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331598 | ||||||
| chr10:59331650
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.325-7544C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331650 | ||||||
| chr10:59331752
|
A | G | 9 | a0001c0001t0001g0092a0001c0001t0001g0153a0001c0001t0001g0191others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-7646T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331752 | ||||||
| chr10:59331847
|
A | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 93 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.325-7741T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331847 | ||||||
| chr10:59331869
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.325-7763A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331869 | ||||||
| chr10:59332056
|
G | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 124 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.325-7950C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332056 | ||||||
| chr10:59332157
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-8051T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332157 | ||||||
| chr10:59332240
|
A | ATG | 6 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG03492.hp1 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-8136_325-8135d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332240 | ||||||
| chr10:59332279
|
T | A | 1 | a0001c0001t0001g0083 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.325-8173A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332279 | ||||||
| chr10:59332733
|
C | T | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(2): Show | 5 | HG02647.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-8627G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332733 | ||||||
| chr10:59333008
|
T | TTTAC | 7 | a0001c0001t0001g0085a0001c0001t0001g0183a0001c0001t0001g0184others(4): Show | 7 | HG02647.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-8903_325-8902i others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333008 | ||||||
| chr10:59333008
|
T | TTTATTTA others(1): Show |
80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(77): Show | 81 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.325-8903_325-8902i others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333008 | ||||||
| chr10:59333008
|
T | TTTATTTA others(5): Show |
3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0174 | 3 | HG00735.hp1 HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.325-8903_325-8902i others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333008 | ||||||
| chr10:59333008
|
T | TTTATTTA others(9): Show |
2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00735.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.325-8903_325-8902i others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333008 | ||||||
| chr10:59333025
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 93 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.325-8919C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333025 | ||||||
| chr10:59333129
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0188 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.325-9023G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333129 | ||||||
| chr10:59333131
|
A | C | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.325-9025T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333131 | ||||||
| chr10:59333252
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.325-9146G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333252 | ||||||
| chr10:59333260
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.325-9154C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333260 | ||||||
| chr10:59333463
|
G | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.325-9357C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333463 | ||||||
| chr10:59333578
|
T | C | 6 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG03492.hp1 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-9472A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333578 | ||||||
| chr10:59333716
|
TTTTA | T | 28 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0153others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.325-9614_325-9611d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333716 | ||||||
| chr10:59333784
|
T | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-9678A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333784 | ||||||
| chr10:59333893
|
T | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-9787A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333893 | ||||||
| chr10:59334164
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 122 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.325-10058G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334164 | ||||||
| chr10:59334421
|
G | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0067others(2): Show | 5 | HG03654.hp1 HG03927.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-10315C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334421 | ||||||
| chr10:59334495
|
C | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 93 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.325-10389G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334495 | ||||||
| chr10:59334507
|
C | A | 2 | a0001c0001t0001g0154a0001c0007t0001g0059 | 2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.325-10401G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334507 | ||||||
| chr10:59334544
|
G | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0070others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-10438C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334544 | ||||||
| chr10:59334567
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(37): Show | 41 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.325-10461T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334567 | ||||||
| chr10:59334623
|
C | T | 28 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0153others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.325-10517G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334623 | ||||||
| chr10:59334747
|
C | T | 11 | a0001c0001t0001g0189a0001c0001t0001g0200a0001c0001t0001g0201others(8): Show | 11 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-10641G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334747 | ||||||
| chr10:59335448
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0188 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.325-11342A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335448 | ||||||
| chr10:59335596
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0188 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.325-11490G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335596 | ||||||
| chr10:59335699
|
C | T | 6 | a0001c0001t0001g0143a0002c0002t0001g0035a0002c0002t0001g0036others(3): Show | 6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-11593G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335699 | ||||||
| chr10:59335829
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.325-11723G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335829 | ||||||
| chr10:59335840
|
A | T | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-11734T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335840 | ||||||
| chr10:59335986
|
G | C | 36 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(33): Show | 36 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.325-11880C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335986 | ||||||
| chr10:59336492
|
C | G | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.325-12386G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336492 | ||||||
| chr10:59336625
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.325-12519A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336625 | ||||||
| chr10:59336721
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.325-12615C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336721 | ||||||
| chr10:59336731
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.325-12625A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336731 | ||||||
| chr10:59336869
|
A | G | 5 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0037others(2): Show | 5 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-12763T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336869 | ||||||
| chr10:59336933
|
C | T | 5 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0037others(2): Show | 5 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-12827G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336933 | ||||||
| chr10:59337075
|
A | G | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-12969T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337075 | ||||||
| chr10:59337165
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.325-13059C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337165 | ||||||
| chr10:59337540
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.325-13434A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337540 | ||||||
| chr10:59337655
|
T | C | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 47 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.325-13549A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337655 | ||||||
| chr10:59337667
|
CT | C | 6 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0200others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-13562delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337667
|
CTT | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0053a0001c0001t0001g0057others(15): Show | 18 | HG00558.hp1 HG00673.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.325-13563_325-1356 others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337667
|
CTTT | C | 103 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0023others(100): Show | 103 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.325-13564_325-1356 others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337667
|
CTTTT | C | 9 | a0001c0001t0001g0024a0001c0001t0001g0084a0001c0001t0001g0113others(6): Show | 9 | HG01070.hp2 HG01123.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-13565_325-1356 others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337667
|
CTTTTT | C | 5 | a0001c0001t0001g0182a0002c0002t0001g0035a0002c0002t0001g0036others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-13566_325-1356 others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337667
|
CTTTTTTT others(3): Show |
C | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-13571_325-1356 others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337667
|
CTTTTTTT others(4): Show |
C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(53): Show | 57 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.325-13572_325-1356 others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337667
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0169a0001c0001t0003g0171 | 2 | HG01070.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.325-13573_325-1356 others(16): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337667
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0002g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.325-13582_325-1356 others(25): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | ||||||
| chr10:59337681
|
T | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-13575A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337681 | ||||||
| chr10:59337773
|
G | A | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 47 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.325-13667C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337773 | ||||||
| chr10:59337805
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-13699C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337805 | ||||||
| chr10:59337959
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.325-13853G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337959 | ||||||
| chr10:59337978
|
C | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(51): Show | 55 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.325-13872G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337978 | ||||||
| chr10:59338001
|
C | T | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 47 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.325-13895G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338001 | ||||||
| chr10:59338100
|
T | C | 125 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(122): Show | 125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.325-13994A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338100 | ||||||
| chr10:59338108
|
G | T | 74 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(71): Show | 74 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.325-14002C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338108 | ||||||
| chr10:59338190
|
T | C | 126 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(123): Show | 126 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.324+14080A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338190 | ||||||
| chr10:59338381
|
T | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.324+13889A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338381 | ||||||
| chr10:59338459
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.324+13811A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338459 | ||||||
| chr10:59338460
|
G | T | 7 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0001g0199others(4): Show | 7 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+13810C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338460 | ||||||
| chr10:59338532
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.324+13738C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338532 | ||||||
| chr10:59338567
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.324+13703C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338567 | ||||||
| chr10:59338639
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0188 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.324+13631A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338639 | ||||||
| chr10:59338687
|
C | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(50): Show | 54 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.324+13583G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338687 | ||||||
| chr10:59338832
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.324+13438C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338832 | ||||||
| chr10:59338840
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.324+13430G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338840 | ||||||
| chr10:59338916
|
C | T | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 47 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.324+13354G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338916 | ||||||
| chr10:59338933
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+13337A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338933 | ||||||
| chr10:59339165
|
G | A | 11 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+13105C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339165 | ||||||
| chr10:59339409
|
G | GA | 126 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(123): Show | 126 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.324+12860dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339409 | ||||||
| chr10:59339795
|
A | G | 75 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(72): Show | 75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+12475T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339795 | ||||||
| chr10:59339819
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+12451T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339819 | ||||||
| chr10:59339970
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.324+12300T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339970 | ||||||
| chr10:59340046
|
C | T | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.324+12224G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340046 | ||||||
| chr10:59340216
|
TA | T | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 47 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.324+12053delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340216 | ||||||
| chr10:59340220
|
A | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.324+12050T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340220 | ||||||
| chr10:59340233
|
T | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.324+12037A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340233 | ||||||
| chr10:59340283
|
T | C | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.324+11987A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340283 | ||||||
| chr10:59340294
|
G | C | 2 | a0001c0001t0001g0025a0001c0001t0003g0034 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.324+11976C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340294 | ||||||
| chr10:59340377
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18956.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.324+11893C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340377 | ||||||
| chr10:59340519
|
C | T | 125 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(122): Show | 125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+11751G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340519 | ||||||
| chr10:59340724
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.324+11546T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340724 | ||||||
| chr10:59340740
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324+11530T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340740 | ||||||
| chr10:59340922
|
T | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0007g0185 | 3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.324+11348A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340922 | ||||||
| chr10:59341112
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(51): Show | 55 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.324+11158G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341112 | ||||||
| chr10:59341180
|
G | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.324+11090C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341180 | ||||||
| chr10:59341322
|
C | T | 74 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(71): Show | 74 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.324+10948G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341322 | ||||||
| chr10:59341465
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.324+10805C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341465 | ||||||
| chr10:59341515
|
C | T | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+10755G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341515 | ||||||
| chr10:59341521
|
C | G | 126 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(123): Show | 126 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.324+10749G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341521 | ||||||
| chr10:59341546
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.324+10724C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341546 | ||||||
| chr10:59341590
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.324+10680C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341590 | ||||||
| chr10:59341604
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.324+10666C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341604 | ||||||
| chr10:59341630
|
G | A | 75 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(72): Show | 75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+10640C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341630 | ||||||
| chr10:59341664
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.324+10606G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341664 | ||||||
| chr10:59341685
|
T | C | 125 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(122): Show | 125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+10585A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341685 | ||||||
| chr10:59341864
|
C | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+10406G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341864 | ||||||
| chr10:59342086
|
A | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.324+10184T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342086 | ||||||
| chr10:59342192
|
A | C | 30 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(27): Show | 30 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.324+10078T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342192 | ||||||
| chr10:59342276
|
A | G | 126 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(123): Show | 126 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.324+9994T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342276 | ||||||
| chr10:59342332
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.324+9938G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342332 | ||||||
| chr10:59342360
|
TA | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.324+9909delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342360 | ||||||
| chr10:59342574
|
C | T | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 47 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.324+9696G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342574 | ||||||
| chr10:59342698
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.324+9572C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342698 | ||||||
| chr10:59342729
|
C | T | 146 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0021others(143): Show | 146 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.324+9541G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342729 | ||||||
| chr10:59342889
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.324+9381A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342889 | ||||||
| chr10:59343021
|
C | T | 146 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0021others(143): Show | 146 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.324+9249G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343021 | ||||||
| chr10:59343340
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(50): Show | 54 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.324+8930A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343340 | ||||||
| chr10:59343421
|
TA | T | 75 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(72): Show | 75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+8848delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343421 | ||||||
| chr10:59343547
|
A | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0007g0185 | 3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.324+8723T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343547 | ||||||
| chr10:59343567
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+8703C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343567 | ||||||
| chr10:59343862
|
C | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(70): Show | 73 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.324+8408G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343862 | ||||||
| chr10:59343872
|
A | G | 14 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG02145.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.324+8398T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343872 | ||||||
| chr10:59343875
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.324+8395A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343875 | ||||||
| chr10:59343910
|
C | A | 2 | a0001c0001t0003g0018a0002c0002t0001g0017 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.324+8360G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343910 | ||||||
| chr10:59343949
|
C | CT | 51 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(48): Show | 51 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.324+8320dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343949 | ||||||
| chr10:59343964
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG01099.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.324+8306A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343964 | ||||||
| chr10:59343968
|
C | CT | 6 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0200others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+8301dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343968 | ||||||
| chr10:59343968
|
CT | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+8301delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343968 | ||||||
| chr10:59343993
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324+8277C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343993 | ||||||
| chr10:59344001
|
G | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+8269C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344001 | ||||||
| chr10:59344023
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.324+8247T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344023 | ||||||
| chr10:59344086
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+8184G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344086 | ||||||
| chr10:59344158
|
T | G | 1 | a0001c0001t0002g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.324+8112A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344158 | ||||||
| chr10:59344200
|
G | A | 73 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(70): Show | 73 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.324+8070C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344200 | ||||||
| chr10:59344211
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+8059G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344211 | ||||||
| chr10:59344234
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.324+8036A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344234 | ||||||
| chr10:59344284
|
CT | C | 42 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.324+7985delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344284 | ||||||
| chr10:59344287
|
T | C | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.324+7983A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344287 | ||||||
| chr10:59344340
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.324+7930C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344340 | ||||||
| chr10:59344427
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.324+7843G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344427 | ||||||
| chr10:59344445
|
A | AT | 112 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(109): Show | 112 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.324+7824dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344445 | ||||||
| chr10:59344445
|
A | ATT | 13 | a0001c0001t0001g0087a0001c0001t0001g0180a0001c0001t0001g0181others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+7823_324+7824d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344445 | ||||||
| chr10:59344528
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.324+7742G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344528 | ||||||
| chr10:59344556
|
A | G | 73 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(70): Show | 73 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.324+7714T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344556 | ||||||
| chr10:59344565
|
A | G | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+7705T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344565 | ||||||
| chr10:59344597
|
A | T | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+7673T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344597 | ||||||
| chr10:59344780
|
G | T | 1 | a0003c0003t0001g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.324+7490C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344780 | ||||||
| chr10:59344822
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+7448T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344822 | ||||||
| chr10:59344835
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.324+7435A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344835 | ||||||
| chr10:59344862
|
C | T | 145 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0021others(142): Show | 145 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.324+7408G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344862 | ||||||
| chr10:59344876
|
G | A | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.324+7394C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344876 | ||||||
| chr10:59344944
|
C | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0190 | 3 | HG00597.hp1 HG00609.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.324+7326G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344944 | ||||||
| chr10:59345032
|
C | T | 4 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0037others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+7238G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345032 | ||||||
| chr10:59345033
|
G | A | 5 | a0001c0001t0001g0172a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+7237C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345033 | ||||||
| chr10:59345188
|
CA | C | 4 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0037others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+7081delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345188 | ||||||
| chr10:59345190
|
T | C | 30 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(27): Show | 30 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.324+7080A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345190 | ||||||
| chr10:59345303
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.324+6967A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345303 | ||||||
| chr10:59345346
|
A | T | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+6924T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345346 | ||||||
| chr10:59345552
|
T | C | 7 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0001g0199others(4): Show | 7 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+6718A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345552 | ||||||
| chr10:59345715
|
A | C | 75 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(72): Show | 75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+6555T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345715 | ||||||
| chr10:59345883
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.324+6387G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345883 | ||||||
| chr10:59346083
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.324+6187C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346083 | ||||||
| chr10:59346137
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.324+6133A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346137 | ||||||
| chr10:59346207
|
T | TAGAAA | 125 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(122): Show | 125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+6058_324+6062d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346207 | ||||||
| chr10:59346222
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.324+6048T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346222 | ||||||
| chr10:59346228
|
T | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+6042A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346228 | ||||||
| chr10:59346237
|
T | C | 75 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(72): Show | 75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+6033A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346237 | ||||||
| chr10:59346340
|
T | C | 10 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0067others(7): Show | 10 | HG03492.hp1 HG03927.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+5930A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346340 | ||||||
| chr10:59346627
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(51): Show | 55 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.324+5643C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346627 | ||||||
| chr10:59346657
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0165a0001c0001t0001g0183others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+5613A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346657 | ||||||
| chr10:59346934
|
C | G | 125 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(122): Show | 125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+5336G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346934 | ||||||
| chr10:59347044
|
G | A | 74 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(71): Show | 74 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.324+5226C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347044 | ||||||
| chr10:59347125
|
A | T | 65 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(62): Show | 65 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.324+5145T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347125 | ||||||
| chr10:59347434
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+4836C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347434 | ||||||
| chr10:59347462
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+4808G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347462 | ||||||
| chr10:59347518
|
A | AT | 6 | a0001c0001t0001g0085a0002c0002t0001g0035a0002c0002t0001g0036others(3): Show | 6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+4751dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347518 | ||||||
| chr10:59347518
|
AT | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0197others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+4751delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347518 | ||||||
| chr10:59347520
|
T | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0025others(75): Show | 78 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.324+4750A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347520 | ||||||
| chr10:59347618
|
G | C | 1 | a0001c0004t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.324+4652C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347618 | ||||||
| chr10:59347644
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG01099.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.324+4626T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347644 | ||||||
| chr10:59347690
|
G | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0165a0001c0001t0001g0183others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+4580C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347690 | ||||||
| chr10:59347884
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.324+4386G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347884 | ||||||
| chr10:59348203
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.324+4067C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348203 | ||||||
| chr10:59348406
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.324+3864G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348406 | ||||||
| chr10:59348644
|
T | G | 1 | a0001c0001t0001g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.324+3626A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348644 | ||||||
| chr10:59348784
|
C | T | 50 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+3486G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348784 | ||||||
| chr10:59348785
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0188 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.324+3485T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348785 | ||||||
| chr10:59348914
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+3356C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348914 | ||||||
| chr10:59349212
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+3058T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349212 | ||||||
| chr10:59349228
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.324+3042A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349228 | ||||||
| chr10:59349325
|
T | C | 3 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG02970.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.324+2945A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349325 | ||||||
| chr10:59349357
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.324+2913C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349357 | ||||||
| chr10:59349602
|
C | CAAA | 49 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+2665_324+2667d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349602 | ||||||
| chr10:59349646
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 180 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.324+2624A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349646 | ||||||
| chr10:59349676
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.324+2594A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349676 | ||||||
| chr10:59349803
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+2467C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349803 | ||||||
| chr10:59349970
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 130 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.324+2300A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349970 | ||||||
| chr10:59349994
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.324+2276A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349994 | ||||||
| chr10:59350010
|
A | C | 74 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(71): Show | 74 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.324+2260T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350010 | ||||||
| chr10:59350066
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.324+2204A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350066 | ||||||
| chr10:59350075
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+2195A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350075 | ||||||
| chr10:59350316
|
G | A | 1 | a0004c0005t0001g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.324+1954C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350316 | ||||||
| chr10:59350618
|
T | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0007g0185 | 3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.324+1652A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350618 | ||||||
| chr10:59350845
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+1425T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350845 | ||||||
| chr10:59350877
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.324+1393A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350877 | ||||||
| chr10:59351013
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.324+1257C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351013 | ||||||
| chr10:59351195
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.324+1075C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351195 | ||||||
| chr10:59351331
|
C | CA | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 60 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.324+938dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | ||||||
| chr10:59351331
|
C | CAA | 72 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(69): Show | 72 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.324+937_324+938dup others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | ||||||
| chr10:59351331
|
C | CAAAA | 7 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0001g0199others(4): Show | 7 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+935_324+938dup others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | ||||||
| chr10:59351331
|
C | CAAAAA | 29 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+934_324+938dup others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | ||||||
| chr10:59351331
|
C | CAAAAAA | 10 | a0001c0001t0001g0056a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG01243.hp2 HG01261.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+933_324+938dup others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | ||||||
| chr10:59351542
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0165 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.324+728C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351542 | ||||||
| chr10:59351588
|
C | T | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 47 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.324+682G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351588 | ||||||
| chr10:59351797
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.324+473G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351797 | ||||||
| chr10:59351986
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 60 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.324+284T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351986 | ||||||
| chr10:59352215
|
G | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 146 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.324+55C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59352215 | ||||||
| chr10:59352534
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120-60T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59352534 | ||||||
| chr10:59352761
|
A | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG02723.hp1 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.120-287T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59352761 | ||||||
| chr10:59352818
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.120-344T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59352818 | ||||||
| chr10:59352893
|
C | T | 29 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.120-419G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59352893 | ||||||
| chr10:59353038
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 173 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.120-564A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353038 | ||||||
| chr10:59353106
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.120-632T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353106 | ||||||
| chr10:59353363
|
C | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 29 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.120-889G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353363 | ||||||
| chr10:59353504
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120-1030A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353504 | ||||||
| chr10:59353519
|
A | C | 30 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(27): Show | 30 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.120-1045T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353519 | ||||||
| chr10:59353610
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 180 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.120-1136T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353610 | ||||||
| chr10:59353681
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0165a0001c0001t0001g0183others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.120-1207A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353681 | ||||||
| chr10:59353765
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 185 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.120-1291T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353765 | ||||||
| chr10:59354067
|
C | CTTTA | 13 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0053others(10): Show | 13 | HG01884.hp2 HG03492.hp1 HG03492.hp2 others(10): Show |
intron_variant | MODIFIER | c.120-1597_120-1594d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354067 | ||||||
| chr10:59354067
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.120-1593G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354067 | ||||||
| chr10:59354075
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.120-1601A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354075 | ||||||
| chr10:59354155
|
CT | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.120-1682delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354155 | ||||||
| chr10:59354213
|
A | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+1674T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354213 | ||||||
| chr10:59354220
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.119+1667A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354220 | ||||||
| chr10:59354233
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 89 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.119+1654C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354233 | ||||||
| chr10:59354474
|
G | A | 1 | a0001c0004t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.119+1413C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354474 | ||||||
| chr10:59354498
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.119+1389G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354498 | ||||||
| chr10:59354745
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.119+1142A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354745 | ||||||
| chr10:59354844
|
T | C | 3 | a0001c0001t0001g0197a0001c0001t0001g0199a0002c0002t0006g0198 | 3 | HG01123.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.119+1043A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354844 | ||||||
| chr10:59354870
|
T | C | 1 | a0001c0001t0002g0068 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.119+1017A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354870 | ||||||
| chr10:59354995
|
C | CAAT | 18 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0186others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.119+889_119+891dup others(3): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354995 | ||||||
| chr10:59355013
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.119+874A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355013 | ||||||
| chr10:59355354
|
C | T | 18 | a0001c0001t0001g0051a0001c0001t0001g0163a0001c0001t0001g0169others(15): Show | 18 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.119+533G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355354 | ||||||
| chr10:59355413
|
A | G | 32 | a0001c0001t0001g0051a0001c0001t0001g0070a0001c0001t0001g0163others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.119+474T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355413 | ||||||
| chr10:59355463
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.119+424T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355463 | ||||||
| chr10:59355532
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.119+355G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355532 | ||||||
| chr10:59355566
|
A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(11): Show | 14 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.119+321T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355566 | ||||||
| chr10:59355657
|
C | A | 1 | a0005c0008t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.119+230G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355657 | ||||||
| chr10:59355722
|
G | A | 15 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(12): Show | 15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.119+165C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355722 | ||||||
| chr10:59355847
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.119+40A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355847 | ||||||
| chr10:59355952
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63-9C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59355952 | ||||||
| chr10:59356377
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.63-434A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356377 | ||||||
| chr10:59356424
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.63-481C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356424 | ||||||
| chr10:59356424
|
G | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-481C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356424 | ||||||
| chr10:59356541
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02965.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.63-598G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356541 | ||||||
| chr10:59356761
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.63-818C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356761 | ||||||
| chr10:59356819
|
C | CGACTCAG others(51): Show |
1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.63-877_63-876insCC others(56): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356819 | ||||||
| chr10:59356824
|
A | T | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.63-881T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356824 | ||||||
| chr10:59356827
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.63-884G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356827 | ||||||
| chr10:59356828
|
T | A | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.63-885A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356828 | ||||||
| chr10:59356847
|
C | T | 15 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(12): Show | 15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-904G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356847 | ||||||
| chr10:59356935
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.63-992G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356935 | ||||||
| chr10:59356949
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63-1006A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356949 | ||||||
| chr10:59356976
|
T | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0179 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.63-1033A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356976 | ||||||
| chr10:59357008
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.63-1065G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357008 | ||||||
| chr10:59357010
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-1067G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357010 | ||||||
| chr10:59357020
|
G | T | 1 | a0001c0001t0001g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63-1077C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357020 | ||||||
| chr10:59357027
|
G | A | 15 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(12): Show | 15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-1084C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357027 | ||||||
| chr10:59357062
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63-1119G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357062 | ||||||
| chr10:59357153
|
T | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.63-1210A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357153 | ||||||
| chr10:59357258
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(10): Show | 13 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-1315A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357258 | ||||||
| chr10:59357282
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG00738.hp1 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-1339A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357282 | ||||||
| chr10:59357341
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-1398T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357341 | ||||||
| chr10:59357374
|
A | G | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63-1431T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357374 | ||||||
| chr10:59357455
|
A | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0007g0185 | 3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.63-1512T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357455 | ||||||
| chr10:59357466
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63-1523T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357466 | ||||||
| chr10:59357645
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-1702A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357645 | ||||||
| chr10:59357841
|
C | T | 17 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(14): Show | 17 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.63-1898G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357841 | ||||||
| chr10:59358053
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(72): Show | 76 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.63-2110A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358053 | ||||||
| chr10:59358072
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63-2129A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358072 | ||||||
| chr10:59358225
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.63-2282T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358225 | ||||||
| chr10:59358291
|
C | T | 17 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(14): Show | 17 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.63-2348G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358291 | ||||||
| chr10:59358295
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(10): Show | 13 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-2352A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358295 | ||||||
| chr10:59358308
|
G | A | 15 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(12): Show | 15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-2365C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358308 | ||||||
| chr10:59358479
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.63-2536C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358479 | ||||||
| chr10:59358532
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.63-2589T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358532 | ||||||
| chr10:59358556
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-2613A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358556 | ||||||
| chr10:59358583
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.63-2640G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358583 | ||||||
| chr10:59358660
|
T | C | 15 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(12): Show | 15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-2717A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358660 | ||||||
| chr10:59358702
|
TC | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-2760delG | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358702 | ||||||
| chr10:59358912
|
C | T | 15 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(12): Show | 15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-2969G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358912 | ||||||
| chr10:59359057
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0152 | 2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.63-3114C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359057 | ||||||
| chr10:59359250
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.62+3149G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359250 | ||||||
| chr10:59359646
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.62+2753A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359646 | ||||||
| chr10:59359656
|
C | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.62+2743G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359656 | ||||||
| chr10:59359934
|
G | A | 15 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(12): Show | 15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.62+2465C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359934 | ||||||
| chr10:59360012
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.62+2387A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360012 | ||||||
| chr10:59360076
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.62+2323G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360076 | ||||||
| chr10:59360124
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.62+2275G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360124 | ||||||
| chr10:59360260
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.62+2139A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360260 | ||||||
| chr10:59360483
|
A | G | 1 | a0001c0004t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.62+1916T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360483 | ||||||
| chr10:59360490
|
A | G | 15 | a0001c0001t0001g0051a0001c0001t0001g0169a0001c0001t0001g0172others(12): Show | 15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.62+1909T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360490 | ||||||
| chr10:59360532
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.62+1867A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360532 | ||||||
| chr10:59360567
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.62+1832T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360567 | ||||||
| chr10:59360724
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(70): Show | 74 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.62+1675G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360724 | ||||||
| chr10:59360853
|
G | GA | 15 | a0001c0001t0001g0006a0001c0001t0001g0155a0001c0001t0001g0156others(12): Show | 15 | HG01071.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.62+1545dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360853 | ||||||
| chr10:59360853
|
GA | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(66): Show | 70 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.62+1545delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360853 | ||||||
| chr10:59360853
|
GAA | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0189others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.62+1544_62+1545del others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360853 | ||||||
| chr10:59360853
|
GAAAAAAA others(7): Show |
G | 11 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173others(8): Show | 11 | HG01070.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.62+1532_62+1545del others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360853 | ||||||
| chr10:59360924
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.62+1475G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360924 | ||||||
| chr10:59360958
|
A | G | 16 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.62+1441T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360958 | ||||||
| chr10:59361212
|
GT | G | 15 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0191others(12): Show | 15 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.62+1186delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361212 | ||||||
| chr10:59361605
|
CAT | C | 19 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173others(16): Show | 19 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.62+792_62+793delAT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361605 | ||||||
| chr10:59361641
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.62+758A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361641 | ||||||
| chr10:59361862
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.62+537C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361862 | ||||||
| chr10:59361986
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62+413G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361986 | ||||||
| chr10:59361995
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+404C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361995 | ||||||
| chr10:59362382
|
T | C | 13 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0197others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.62+17A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59362382 |